Ethyl 2-bromopropionate Research Articles

Synthesis of Ultrahigh Molecular Weight Poly (Trifluoroethyl Methacrylate) Initiated by the Combination of Palladium Nanoparticles with Organic Halides

Ultrahigh molecular weight polymers display outstanding properties and have great application potential. However, the traditional polymerization methods have inevitable disadvantages that challenge the green synthesis of ultrahigh molecular weight polymers. The paper achieved an ultrahigh molecular weight poly (trifluoroethyl methacrylate) via a novel polymerization and discussed the mechanistic, kinetic, and experimental aspects. The combination of palladium nanoparticles with ethyl 2-bromopropionate has been identified as an exceedingly efficient system for initiating the polymerization of trifluoroethyl methacrylate. An ultrahigh molecular weight poly (trifluoroethyl methacrylate) with a number-average molecular weight up to 3.03 × 106 Da has been synthesized at a feeding molar ratio of [poly (trifluoroethyl methacrylate)]/[ethyl 2-bromopropionate]/[palladium nanoparticles] = 3.95 × 104:756:1 at 70 °C. The reaction orders concerning palladium nanoparticles, ethyl 2-bromopropionate, and poly (trifluoroethyl methacrylate) were determined to be 0.59, 0.34, and 1.38, respectively. By analyzing a series of characterizations, we verified that the polymerization of poly (trifluoroethyl methacrylate) was initiated by the ethyl 2-bromopropionate residue radicals, which were generated from the interaction between palladium nanoparticles and ethyl 2-bromopropionate. The comparatively large size of the palladium nanoparticles provided a barrier to chain-growing radicals, promoting the synthesis of ultrahigh molecular weight polymers.

Where is the induction from? Effect of disproportionation and comproportionation in Cu(0)-mediated reversible deactivation radical polymerization

There is a controversial debate about the mechanism of reversible deactivation radical polymerization (RDRP) in the presence of Cu(0). Two mechanism models have been proposed - supplemental activator and reducing agent atom transfer radical polymerization (SARA ATRP) and single-electron transfer living radical polymerization (SET-LRP), however, they are contradictory to each other, and neither of them are able to fully explain experimental phenomenon in the Cu(0)-mediated RDRP process, especially a period of slow addition i.e., induction period occurs under certain reaction conditions. In this work, the induction phenomenon and its underlying mechanism was explored and clarified by using different catalyst systems (CuI, Cu(0), Cu(0)&CuII) and different initiator systems i.e., EBriB (ethyl α-bromoisobutyrate), EBrP (ethyl 2-bromopropionate), MBrP (methyl 2-bromopropionate) and MClP (methyl 2-chloropropionate). New insights on the roles of different copper species and their mutual conversion kinetics were provided. It is proved that the appearance/absence of the induction period is due to the difference in the relative concentrations of CuI and CuII accumulated at the early stage of the reaction. Moreover, the disproportionation and comproportionation co-exist in the Cu(0)-mediated RDRP system and play an essential role in establishing the equilibrium among different copper species (Cu0, CuI and CuII) at the early reaction stage.

Separation of chiral compounds using high performance liquid chromatography stationary phase based on covalent organic framework material TpPa-NH2-Glu

Covalent organic frameworks （COFs） are an emerging class of porous crystalline materials composed of multidentate organic units connected by covalent bonds. COFs have been demonstrated to exhibit great potential and research value in many fields， including gas storage and separation， photoelectric devices， fluorescence sensors， catalysis， drug delivery， dye and pollutant adsorption， and electronic devices， and so on. The COFs obtained by post-synthesis modification tend to exhibit high crystallinities and porosities， thereby rendering them suitable materials for use in the fields of chiral resolution， asymmetric catalysis， and chromatography. In this work， TpPa-NO2 was synthesized from 1，3，5-tricarbaldehyde phloroglucinol and 2-nitro-1，4-phenylenediamine， which was then reduced to TpPa-NH2. Subsequently， this material was modified with D-glucose via a post-synthesis modification strategy to obtain the TpPa-NH2-Glu. TpPa-NH2-Glu were characterized by nuclear magnetic resonance （NMR） spectroscopy， Fourier transform-infrared （FT-IR） spectroscopy， X-ray powder diffraction （XRD） analysis， etc. In the XRD pattern， the peaks observed at 4.7°， 8.1°， 11.1°， and 27° were attributed to the TpPa-NH2-Glu， and these peaks are consistent with previous reports， thereby confirming the successful synthesis of this derivative. In addition， circular dichroism experiments indicated that the TpPa-NH2-Glu exhibited a Cotton effect， further confirming the chiral COF was prepared. Subsequently， this material was immobilized on the surface of spherical silica gel particles via the net-wrapping method to prepare a stationary phase for high performance liquid chromatographic column. Using n-hexane-isopropanol （9∶1， v/v） or methanol-water （9∶1， v/v） as mobile phases at a flow rate of 0.5 mL/min， 16 racemates and two benzene-based positional isomers （o，m，p-nitroaniline and o，m，p-Iodoaniline） were successfully resolved by this chiral column. In addition， under methanol-water （9∶1， v/v） mobile phase conditions， five racemates were separated， among which propranolol hydrochloride， warfarin， and metoprolol reached baseline separation. Furthermore， under n-hexane-isopropanol （9∶1， v/v） mobile phase conditions， 11 racemates were resolved， among which ethyl 2-bromopropionate and 3-butyn-2-ol reached baseline separation. Meanwhile， the effect of temperature on the TpPa-NH2-Glu liquid chromatography column and the repeatability of the TpPa-NH2-Glu liquid chromatography column were also explored. The HPLC column prepared by TpPa-NH2-Glu had good repeatability， and its relative standard deviation （RSD） was 1.55% and 1.46%， respectively. It is demonstrated that the TpPa-NH2-Glu material has good resolution ability for chiral compounds.

In Situ Generated Crude Trithiocarbonate for Visible Light‐Mediated RAFT Polymerization of Acrylates**

AbstractReversible addition‐fragmentation chain transfer (RAFT) radical polymerization holds great promise in the design and massive production of functional polymeric materials. However, its practical application was restricted by the scale‐up production of chain transfer agents, the insufficient oxygen tolerance, and its environmental impact. In this work, a trithiocarbonate (TTC)‐based RAFT agent ethyl 2‐(((butylthio)carbonothioyl)thio)propanoate was synthesized in situ using shelf‐stable RAFT precursors, i. e., sodium n‐butyl trithiocarbonate (TTCS) and ethyl 2‐bromopropionate (EBrP). The crude product was then directly used in RAFT polymerization of acrylates under the irradiation of LED at 405 nm. First‐order polymerization kinetics was evidenced by proton nuclear magnetic resonance and size exclusion chromatography analysis. The measured molecular weights were close to the theoretical values and the dispersities of poly(tert‐butyl acrylate)s (PtBAs) are as low as 1.08, thanks to the light‐induced activation of the RAFT agent. Well‐defined PtBA is also obtained in the presence of air, due to the intrinsic catalytic behavior of TTC. The proposed method greatly simplifies the set‐up of RAFT polymerization without compromising its control for the polymerization. And it also contributes to reducing the cost and environmental impact of the RAFT polymerization, being promising for the industrialization of RAFT polymerization.

Synthesis and Characterization of Benzodioxinone-Bearing Methacrylate-Based Random Copolymer via Atom Transfer Radical Polymerization

Methacrylate-benzodioxinone (BDMA) as a monomer was firstly synthesized and then copolymerized with methyl methacrylate and 2-hydroxyethyl methacrylate via atom transfer radical polymerization (ATRP) in the presence of CuCl/pentamethyldiethylene triamine (PMDETA) catalytic system using ethyl 2-bromopropionate (EtBrP) as an initiator. Successful formation of the block copolymer was also confirmed in detail by proton nuclear magnetic resonance spectroscopy (1H NMR), Fourier-transform infrared spectroscopy (FT-IR), and gel permeation chromatography (GPC) appropriately. Secondly, photochemical acylation of obtained copolymer through hydroxyl and benzodioxinone groups led to the release of benzophenone compound and ester-linkage on the polymer backbone. The formation of ester-linkage increases the glass transition temperature and the thermal stability of the obtained copolymer.

PH-Sensitive betulinic acid polymer prodrug nanoparticles for efficient and targeted cancer cells treatment

pH-sensitive betulinic acid (BA) polymer prodrug nanoparticles, have been proposed. The carboxyl group-terminated poly[2-(3-butenyl)-2-oxazoline] (PBuOx-COOH) is prepared by cationic ring-opening polymerization (CROP) of the 2-(3-butenyl)-2-oxazoline (BuOx) using ethyl 3-bromopropionate as initiator followed by hydrolysis with methanolic KOH. Folic acid (FA) was connected with the PBuOx-COOH through polyethylene glycol (PEG) as spacer forming the FA-PEG-PBuOx. Thiol-modified betulinic acid (BA-SH) is conjugated to the side chains of FA-PEG-PBuOx by thio-ene reaction endowed the FA-PEG-PBuOx/BA with the acid-liable β-thiopropionate linkages. Additionally, the cellular uptake of the prodrug nanoparticles also showed vital potential for folate-receptor-positive HeLa cells.

Fast acquisition of high-resolution 2D NMR spectroscopy in inhomogeneous magnetic fields

High-resolution nuclear magnetic resonance (NMR) spectroscopy plays an important role in chemical and biological analyses. In this study, we combine the J-coupling coherence transfer module with the echo-train acquisition technique for fast acquisition of high-resolution 2D NMR spectra in magnetic fields with unknown spatial variations. The proposed method shows satisfactory performance on a 5mM ethyl 3-bromopropionate sample, under a 5-kHz (10ppm at 11.7T) B0 inhomogeneous field, as well as under varying degrees of pulse-flip-angle deviations. Moreover, a simulative ex situ NMR measurement is also conducted to show the effectiveness of the proposed pulse sequence.

Atom transfer radical polymerization and copolymerization of isoprene catalyzed by copper bromide/2,2′-bipyridine

Abstract ATRP, as one of the most successful controlled/“living” radical polymerization techniques, has been applied to a large variety of monomers including styrenes, (meth)acrylates, (meth)acrylamides, acrylonitrile, and vinyl acetate. However, ATRP of isoprene still remains a challenge due to poor solubility of copper catalysts in isoprene and low chain propagation rate constant of the monomer. In this work, CuBr/2,2′-bipyridine was found to effectively mediate ATRP of isoprene at 100 °C, 130 °C, and 150 °C with ethyl 2-bromopropionate as an initiator. The polymerizations proceeded smoothly and reached 48.1%, 53.3%, and 71.0% conversions, respectively, in 72 h, producing polyisoprenes with molecular weights close to theoretical values and relatively narrow distributions. A block copolymer of polystyrene-b-polyisoprene was prepared using CuBr/2,2″-bipyridine as a catalyst and polystyrene as a macroinitiator. The 1 H NMR and 13 C NMR analysis of polyisoprene indicated that the polymer had 88.8% 1,4-addition structure and 63.9% of the polymer backbone units were in trans-configuration.

A heteronuclear intermolecular single-quantum coherence scheme for high-resolution 2D J-resolved 1H NMR spectra in inhomogeneous magnetic fields

ABSTRACTBased on heteronuclear intermolecular single-quantum coherences between proton (1H) and quadrupolar nuclei (i.e. deuterium 2H), a three-dimensional nuclear magnetic resonance (NMR) pulse sequence is proposed for recovering high-resolution two-dimensional J-resolved NMR spectra from samples mixed with a deuterated solvent in the presence of large magnetic field inhomogeneities. Benefitting from excitation of spins via two different radio frequency (RF) transmit channels, this sequence is suitable for applications in randomly large inhomogeneous fields and the solvent suppression generally required in homonuclear intermolecular multiple-quantum coherence approaches is no longer necessary. Systematic theoretical analyses are given based on the distant dipolar field treatment. Experiment on a sample of corn oil in deuterated acetone and ethyl 3-bromopropionate and acetone dissolved in DMSO-d6 in a deshimmed field with severe inhomogeneous broadening is performed to show the feasibility and applicability of this sequence.

Optimizing Activators Regenerated by Electron Transfer for Atom Transfer Radical Polymerization of Methyl Methacrylate Initiated by Ethyl 2-bromopropionate

In this study, we used ethyl 2-bromopropionate (EBrP) as an initiator of activators regenerated by electron transfer for atom transfer radical polymerization (ARGET ATRP) of methyl methacrylate (MMA). We investigated in detail the effect on polymerization of different kinds of reducing agents and ligands, the amounts of the reducing agent and catalyst, and reaction temperature. We determined the molecular weight and dispersity of the polymers by gel permeation chromatography (GPC). The results reveal glucose to be the best reducing agent for this system. The monomer conversion increased with increases in the reaction temperature and in the feeding amounts of the reducing agent and catalyst. The optimum amount of the reducing agent and minimal amount of catalyst required depend on the particular system. For example, we polymerized MMA with 200 ppm of catalyst and 15-fold of glucose/CuCl2 resulting in a PMMA with high Mn (Mn,GPC = 48 700, Mn,theo = 48 500) and low dispersity (1.27). The first-order kinetics show that the molecular weights increased linearly with the monomer conversion and are consistent with the theoretical values, the chain extension reaction and end group analysis results also demonstrate that the characteristics of polymerization process belong to a typical “living”/controlled radical polymerization. Moreover, 1H-NMR analysis results indicate the stereoregularity of the polymer is given priority over syndiotactic architecture and the effect of the type of ligand on the stereoregularity is very slight.

Scope and mechanism of the electrochemical Reformatsky reaction of α-haloesters on a graphite powder cathode in aqueous anolyte

Six α-haloesters and eighteen carbonyl compounds were submitted to electrochemical coupling on a graphite powder cathode using aqueous anolyte free of organic solvents. Preparative yields of coupling products could be obtained with ethyl 2-bromoisobutyrate and aromatic aldehydes. Ethyl 2-bromopropionate was much less efficient. Extensive variation of applied potential, electrolyte composition, stoichiometry, catalyst, leaving halogen and activating substituents on the carbonyl compound led to the conclusion that the reaction mechanism in most cases proceeds via a radical intermediate generated from the halide reduction. Ethyl chloroacetate produced only trace amounts of coupling product, most probably by a carbanionic mechanism.

Synthesis, NMR spectral and antimicrobial studies of some [N-methyl-3t-alkyl-2r,6c-diarylpiperidin-4-ylidine]-5′-methylthiazolidine-4-ones

Four new [N-methyl-3t-alkyl-2r,6c-diaryl-4-ylidine]-5′-methylthiozolidin-4-ones 9–12 have been synthesized by the condensation of N-methyl-3t-alkyl-2r,6c-diarylpiperidin-4-one thiosemicarbazones with ethyl 2-bromopropionate. These compounds have been characterized using FT-IR, 1H NMR, 13C NMR spectral techniques. HOMOCOSY, HSQC and HMBC spectral study have been done for [N-methyl-3,3-dimethyl-2r,6c-bis(p-methoxyphenyl)piperidin-4-ylidine]-5′-methylthiazolidine-4-one (12). Two geometrical isomers are formed in this reaction. In all these compounds piperidin rings adopt chair conformation. The rotation of the aryl group at C-2 is rather slow in 10–12. Antimicrobial activities have also been studied for 9–12. These compounds are active against all the tested bacterial and fungal strains.

A kinetic study of atom transfer radical polymerization of styrene with bis(2-pyridyl)ethylenedimethanimine derivative ligands

Atom transfer radical polymerization (ATRP) of styrene was carried out with multidentate nitrogen-based ligands, namely N,N'-bis[phenyl(pyrid-2-yl)methylene] ethane-1,2-diamine (BPDA) and N,N'-bis[methyl(pyrid-2-yl)methylene] ethane-1,2-diamine (BMDA), and catalyst systems at catalyst/ligand molar ratios of 1/0.33, 1/0.5, 1/1, and 1/1.5 by using 2 different initiators, (1-bromoethyl)benzene (BEB) and ethyl-2-bromopropionate (EBP). Linear first-order kinetic plots were observed for ATRP of styrene upon using BPDA as a ligand with both initiators. Even though the linear slopes indicate that radical concentration remains constant during reactions, high molecular weights were obtained at low conversion and showed a linear relation thereafter. To investigate the molecular weight effect, reactions were also performed in the presence of (1-bromoethyl)benzene initiator in dimethylformamide (DMF) for BPDA and in toluene for BMDA using a catalyst/ligand ratio of 1/1.

Determination of ATRP Equilibrium Constants under Polymerization Conditions.

Atom transfer radical polymerization (ATRP) equilibrium constants (KATRP) were measured during polymerization of methyl acrylate (MA) with CuIBr/CuIIBr2 in either dimethyl sulfoxide (DMSO) or acetonitrile (MeCN) in the presence of either tris(2-pyridylmethyl)amine (TPMA) or tris[2-(dimethylamino)ethyl]amine (Me6TREN) as the ligand and with ethyl 2-bromopropionate as the initiator. The ln(KATRP) values changed linearly with the volume fraction of solvents in the reaction medium, allowing extrapolation of the values for KATRP to bulk conditions, which were 2 × 10-9 and 3 × 10-8 for TPMA and Me6TREN ligands at 25 °C, respectively. The temperature effect on KATRP values was studied in MA/MeCN = 1/1 (v/v) with TPMA as the ligand in the temperature range from 0 to 60 °C. The KATRP values increased with temperature providing ΔH = 36 kJ mol-1 in MeCN.

Synthesis, Antimicrobial, and Anti-inflammatory Activities of Novel 2-[3-(1-Adamantyl)-4-substituted-5-thioxo-1,2,4-triazolin-1-yl]acetic Acids, 2-[3-(1-Adamantyl)-4-substituted-5-thioxo-1,2,4-triazolin-1-yl]propionic Acids and Related Derivatives

The reaction of 3-(1-adamantyl)-4-substituted-1,2,4-triazoline-5-thiones 3a-g with sodium chloroacetate, in ethanolic sodium hydroxide yielded the corresponding N1-acetic acid derivatives 4a-g. The interaction of 3a-g with ethyl 2-bromopropionate in acetone, in the presence of potassium carbonate, yielded the corresponding N1-ethyl propionate derivatives 5a-g, which upon hydrolysis with aqueous sodium hydroxide afforded the corresponding propionic acid derivatives 6a-g. Similarly, the reaction of 3-(1-adamantyl)-4-amino-1,2,4-triazoline-5-thione 7 with sodium chloroacetate in ethanolic sodium hydroxide yielded the corresponding N1-acetic acid derivative 8. On the other hand, the reaction of 2-(1-adamantyl)-1,3,4-oxadiazoline-5-thione 9 with sodium chloroacetate yielded the corresponding S-acetic acid derivative 10. Compounds 4a-g, 5b, 5c, 5g, 6a-g, 8 and 10 were tested for in vitro activities against a panel of Gram-positive and Gram-negative bacteria and the yeast-like pathogenic fungus Candida albicans. Several derivatives produced good or moderate activities particularly against Bacillus subtilis. In addition, the in vivo anti-inflammatory activities of these compounds were determined using the carrageenin-induced paw oedema method in rats. Compounds 4a, 4b, 4e, 4f, 6f, 6g and 10 produced good dose-dependent anti-inflammatory activities.

ChemInform Abstract: High Yield Phase Transfer N-Alkylation of Some Benzodiazepines by Esters of ω-Halo Acids.

Abstract Different i, 4-benzodiazepinyl acetic and propionic acids were prepared by hydrogenolysis of benzyl or hydrolysis of the corresponding ethyl esters which were obtained by phase transfer alkylation of respective amides with benzyl bromoacetate and benzyl or ethyl 2-bromopropionate.

Prediction and Experimental Characterization of the Molecular Architecture of FRP and ATRP Synthesized Polyacrylate Networks

AbstractSummary: This work reports experimental and modeling studies concerning the conventional (FRP) and atom transfer radical polymerization (ATRP) of acrylate/diacrylate monomers. In the framework of a recently developed general approach, kinetic models including crosslinking reactions and branching by chain transfer to polymer are discussed for FRP and ATRP polymerization systems. Besides molecular weight distribution (MWD), fairly good predictions of the z‐average radius of gyration could be obtained for these non‐linear polymers. A set of experiments was performed at 1 L scale in a batch reactor using n‐butyl acrylate (BA) or methyl acrylate (MA) as monovinyl monomers and 1,6‐Hexanediol diacrylate (HDDA) or bisphenol A ethoxylate diacrylate (BEDA) as crosslinkers. In FRP experiments, AIBN was used as initiator and ATRP polymerizations were initiated by ethyl 2‐bromopropionate (EBrP) and mediated by CuBr using PMDETA (N,N,N′,N″,N″‐pentamethyldiethylenetriamine) as ligant. Polymerizations were carried out in solution at 60 °C with different dilutions using toluene and DMF as solvents. Products formed at different polymerization times were analyzed by SEC/RI/MALLS yielding average MW, MWD, z‐average radius of gyration and monomer conversion. Important differences in the molecular architecture of the synthesized FRP and ATRP highly branched polyacrylates have been identified. Comparisons of experimental results with predictions have put into evidence the important effect of intramolecular cyclizations at all dilutions, even with ATRP polymerizations.

Synthesis and antimicrobial evaluation of new 3-alkyl/aryl-2-[((α,α-diphenyl-α-hydroxy)acetyl)hydrazono]-5-methyl-4-thiazolidinones

New 4-thiazolidinone derivatives of benzilic acid (alpha,alpha-diphenyl-alpha-hydroxyacetic acid) have been synthesized and evaluated for antibacterial and antifungal activities. The reaction of 1- (alpha,alpha-diphenyl-alpha-hydroxy)acetyl-4-alkyl/arylthiosemicarbazides with ethyl 2-bromopropionate gave 3-alkyl/aryl-2-[((alpha,alpha-diphenyl-alpha-hydroxy)acetyl)hydrazono]-5-methyl-4-thiazolidinone derivatives. Their antibacterial and antifungal activities were evaluated against S. aureus ATCC 29213, P. aeruginosa ATCC 27853, E. coli ATCC 25922, C. albicans ATCC 10231, C. parapsilosis ATCC 22019, C. krusei ATCC 6258, T. mentagrophytes var. erinacei NCPF 375, M. gypseum NCPF 580 and T. tonsurans NCPF 245. 3e, 3f, 3g and 3h showed the highest antibacterial activity. Particularly 3a and 3e showed the highest antifungal activities against C. parapsilosis ATCC 22019, T. tonsurans NCPF 245 and M. gypseum NCPF 580.

Synthesis of well-defined norbornene–lactone-functionalized polymers via ATRP

Well-defined norbornene–lactone-functionalized polymers were synthesized by atom transfer radical polymerization (ATRP) of 5-methacryloxy-6-hydroxynorbornene-2-carboxylic-6-lactone (MNL) and 5-acryloxy-6-hydroxynorbornene-2-carboxylic-6-lactone (ANL) monomers. The ATRP of MNL initiated by ethyl 2-bromopropionate (EBrP), in both N,N-dimethylformamide (DMF) and o-dichlorobenzene (ODCB) solvents was successfully carried out in the presence of CuCl/CuBr and N,N,N′′,N′′,N′′-pentamethyltriethylenetetramine (PMDETA) at 70 °C. The CuCl/ODCB catalyst system gave rise to a lower M w/M n (≦1.20) than CuBr/DMF catalyst system. The ATRP of ANL was feasible in the presence of CuBr and PMDETA at 70 °C but showed lower reactivity than MNL. The resulting polymers were characterized by means of gel permeation chromatography (GPC) and 1H NMR spectroscopy.

Synthesis of 3-(4-Chloro-2-methoxy-7H-pyrrolo[2,3-d]-pyrimidin-7-yl)propanoic acid – An N(9)-Functionalized 7-Deazapurine

Regioselective N-alkylation of 4-chloro-2-methoxy-7H-pyrrolo[2,3- d]pyrimidine (6) with ethyl 3-bromopropionate under liquid-liquid phase-transfer reactionconditions gave the ester 7a. Its saponification yielded the acid 7b. The logP values of a series of N(9)-functionalized purines and purine isosteres were calculated.