Intramolecular Aromatic Substitution Reaction Research Articles

Experimental and Theoretical Investigation of an Azaoxyallyl Cation-Templated Intramolecular Aryl Amination Leading to Oxindole Derivatives.

Herein, development and detailed investigation of a SN '-type intramolecular aromatic substitution reaction involving α-arylazaoxyallyl cation intermediate, is disclosed. The study showcased that while α-aryl-α-chlorohydroxamate could be activated by a combination of base and 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) into the corresponding azaoxyallyl cations, it could further emerge into a π-extended species involving the adjacent α-aryl moiety, and this transition is contingent on electronic effects of the aromatic ring as well as on α-substituents. An effective activation of the α-aromatic ring could pave the path for intramolecular Ar(Csp2 )-N bond formation towards oxindoles. Control experiments and DFT calculations suggested that a non-pericyclic nucleophilic amination pathway is most likely operative and precluded the possibility of concerted or electrophilic amination mechanism. HFIP as the reaction solvent plays pivotal roles in the transformation.

Selective Cu-Catalyzed Intramolecular Annulation of 3-Aryl/Heteryl-2-(diazoacetyl)-1H-pyrroles: Synthesis of Benzo/Furo/Thieno[e]-Fused 1H-Indol-7-oles and Their Transformations.

The Co(III)-catalyzed reaction of 1,3-dicarbonyl compounds with 2-(diazoacetyl)-2H-azirines, prepared by a simplified procedure from 2H-azirin-2-carbonyl chlorides, led in high yields to the formation of 2-(diazoacetyl)pyrroles, while leaving the diazoacetyl function intact. The intramolecular aromatic substitution reaction of 2-(diazoacetyl)pyrroles, catalyzed by Cu(OTf)2, provided selectively previously unknown benzo[e]- and hetero[e]-fused indol-7-oles in good yields. Formylation of benzo[e]indol-4-ol led selectively to the 5-formyl derivative, which is a good precursor for an unusual salen ligand and its Ni-complex. Triflates prepared from benzo[e]indol-4-oles gave various 4-substituted benzo[e]indoles carrying aryl, 2-thienyl, 2-pyridyl, and alkynyl groups, in excellent yields using cross-coupling reactions. 4-(2-Pyridyl)benzo[e]indoles, upon treatment with BF3·Et2O/Et3N, afforded a new type of fluorescent boron complexes with large Stokes shifts.

A Hetero Diels–Alder Approach to the Synthesis of Chromans (3,4-Dihydrobenzopyrans) Using Oxonium Ion Chemistry: The Oxa-Povarov Reaction

An oxa analogue of the well-known Povarov reaction has been developed for the synthesis of 3,4-dihydrobenzopyrans (chromans). The reaction involves the formal inverse electron demand [4 + 2] cycloaddition reaction of in situ-generated cationic aryl 2-oxadiene oxocarbenium ions with alkenes. The oxonium ion intermediates are generated through Lewis acid (SnCl(4))-promoted reactions of phenol-derived Rychnovsky-type mixed acetals. The yield and diastereoselectivity of the chroman products are found to depend upon the substitution pattern of the precursor alkene (i.e., monosubstituted, trans- or cis-disubstituted and cyclic alkenes). Generally, the reactions afford the endo-diastereomers as the major products, except for the reactions of trans-β-methylstyrene, which afford exo-chromans. A comparison of the product distributions from the reactions of trans- and cis-β-methylstyrene reveal that the reaction proceeds, at least in part, by a nonconcerted ionic pathway. Just as for the aza-Povarov reaction, there are two potential mechanisms for the reaction. The first mechanism involves a direct asynchronous [4 + 2] cycloaddition pathway, while the second occurs through the stepwise Prins addition of the alkene to the aryl 2-oxadiene oxonium ion, followed by an intramolecular aromatic substitution reaction of the resultant cation (i.e., a domino Prins/intramolecular Friedel-Crafts reaction).

Synthesis, chemo-selective properties of substituted 9-aryl-9H-fluorenes from triarylcarbinols and enantiomerical kinetics of chiral 9-methoxy-11-(naphthalen-1-yl)-11H-benzo[a]fluorene

9-Aryl-fluorenes were synthesized conveniently from triarylcarbinols in the presence of TsOH. Notably, the orientation of the intramolecular aromatic substitution reaction was dictated by the nature of the substituents on the aryl rings of triarylcarbinols, owing to electronic and conjugated effects. In particular, triarylcarbinols with (3-methoxy)phenyl and naphthalenyl groups formed benzo[a]fluorenes selectively. Moreover, 9-methoxy-11-(naphthalen-1-yl)-11H-benzo[a] fluorene (2g), with a center of chirality, exists as a mixture of diastereoisomers, due to the restricted rotation of a C–C single bond. First-order rate constants for the enantiomerization of 2g in DMSO were obtained over the temperature from 297 K to 393 K, and thermodynamic parameters were determined as ΔH‡ = 99.7 kJ mol−1, ΔS‡373 K = 37.7 J mol−1 K−1, and ΔG‡373 K = 85.6 kJ mol−1 by Eyring plot analysis.

Activation of Electrophilicity of Stable Y-Delocalized Carbamate Cations in Intramolecular Aromatic Substitution Reaction: Evidence for Formation of Diprotonated Carbamates Leading to Generation of Isocyanates

Although cations with three heteroatoms, such as monoprotonated guanidine and urea, are stabilized by Y-shaped conjugation and such Y-conjugated cations are sufficiently basic to be further protonated (or protosolvated) to dications in strongly acid media, only O-monoprotonated species have been detected in the case of carbamates even in magic acid. We found that the trifluoromethanesulfonic acid-catalyzed cyclization of arylethylcarbamates proceeds to afford dihydroisoquinolones in high yield. In strong acids, methyl carbamates are fully O-monoprotonated, and these monocations do not undergo cyclization even under heating. But, as the acidity of the reaction medium is further increased, the cyclization reaction of methyl phenethylcarbamates starts to proceed as a first-order reaction, with a linear relationship between rate and acidity. The sign and magnitude of the entropy of activation ΔS(‡) were found to be similar to those of other A(Ac)1 reactions. These results strongly support the idea that further protonation of the O-protonated carbamates is involved in the cyclization, but the concentration of the dications is very low and suggests that the rate-determining step is dissociation of methanol from the diprotonated carbamate to generate protonated isocyanate, which reacts with the aromatic ring. Therefore, O-protonated carbamates are weak bases in sharp contrast to other Y-shaped monocations.

P−C Bond Activation Chemistry: Evidence for 1,1-Carboboration Reactions Proceeding with Phosphorus−Carbon Bond Cleavage

A series of diarylphosphinyl-substituted acetylenes of the type (aryl)(2)P-C≡C-R (aryl = phenyl or mesityl, R = Ph or n-propyl) react with the strongly Lewis acid reagent B(C(6)F(5))(3) in toluene at elevated temperatures (70-105 °C) to give the 1,1-carboboration products 4. Treatment of bis(diphenylphosphinyl)acetylene with B(C(6)F(5))(3) under analogous conditions proceeded with phosphinyl migration to yield the 1,1-carboboration product 4d, bearing a geminal pair of Ph(2)P substituents at one former acetylene carbon atom and a C(6)F(5) substituent and the remaining -B(C(6)F(5))(2) group at the other. Prolonged thermolysis of 4d resulted in an intramolecular aromatic substitution reaction by means of Ph(2)P attack on the adjacent C(6)F(5) ring to yield the zwitterionic phospha-indene derivative 7. The compounds 4a, 4c, 4d, and 7 were characterized by X-ray diffraction.

Intramolecular Benzylic Cyclization with Nitrenium Ions Generated from N-Acylaminophthalimides Using Phenyliodine(III) Bis(trifluoroacetate): Formation of Phenyl Substituted Lactams

N-Phthalimido-N-acylnitrenium ions generated from N-acylaminophthalimides using phenyliodine(III) bis(trifluoroacetate) in polyfluoro alcohols do not undergo intramolecular aromatic substitution reactions. Instead, intramolecular cyclization to the benzylic position occurs to afford lactams having a phenyl group substituted at the α-position to the ring nitrogen. These reactions proceed in moderate to good yields.

Synthesis of Methyl (E)‐2‐Nitromethylcinnamates Derived from Baylis—Hillman Acetates and Conversion into Several Coumarin Derivatives.

Fast and easy access to methyl (E)-2-nitromethylcinnamates, from the corresponding Baylis-Hillman acetates with NaNO 2 in DMF is described. Several ortho-chloro-2-nitromethylcinnamates undergo intramolecular aromatic substitution reaction followed by rearrangement to yield coumarin derivatives.

Synthesis of Methyl (E)-2-Nitromethylcinnamates Derived from Baylis-Hillman­ Acetates and Conversion into Several Coumarin Derivatives

Fast and easy access to methyl (E)-2-nitromethylcinnamates, from the corresponding Baylis-Hillman acetates with NaNO 2 in DMF is described. Several ortho-chloro-2-nitromethylcinnamates undergo intramolecular aromatic substitution reaction followed by rearrangement to yield coumarin derivatives.

Ortho Effects in the Dissociation of Ionized N-Chlorophenyl- and N-Bromophenyl-2-Aminobenzamidines: Intramolecular Aromatic Substitution with Cyclization to Protonated 2-(2-Aminophenyl)-1H-Benzimidazoles

Electron ionization (70 eV) mass spectra, double-stage (MS2) 10 eV collision-induced dissociation (CID) product-ion mass spectra of molecular ions and triple-stage (MS3) sequential product-ion mass spectra of major fragment ions are reported for the parent N-phenyl and the isomeric ortho-, meta- and para- N-chlorophenyl- and N-bromophenyl-2-aminobenzamidines. Dissociation is greatly influenced by an ortho effect that favors the loss of ortho H atoms and particularly the loss of the ortho halogen substituents. Dissociation occurs via a two-step intramolecular aromatic substitution reaction and a distonic-ion intermediate inhibits scrambling of ring hydrogens thus favoring the loss of the ortho substituents. The ortho isomers form an abundant and diagnostic [M – X]+ fragment ion (X = Cl, Br) and are easily distinguished. Protonated 2-(1 H-benzimidazol-2-yl)-phenylammonium ions are likely formed; they dissociate mainly by NH3 loss upon CID and react readily with pyridine by proton transfer.

Minor aristolochic acids from Aristolochia argentina and mass spectral analysis of aristolochic acids

The minor aristolochic acids isolated from Aristolochia argentina were identified as 6,7-dimethoxy, 6-hydroxy-7-methoxy, 2-hydroxy-8-methoxy and 7-hydroxy-8-methoxy disubstituted derivatives of the 3,4-methylenedioxy-10-nitro-1-phenanthroic acid, respectively. A. argentina also contains the previously reported aristoloside. The mass spectra of the aristolochic acids, their esters and decarboxylation products have been examined. A number of successive fragmentation processes leading to the formation of aromatic hydrocarbons were observed. Cleavage of the nitro group is a prominent process in the mass spectra of the aristolochic acids and their esters. Evidence is presented that the formation of the [MNO 2] + ion occurs by an intramolecular aromatic substitution reaction with participation of the CO 2R group. The different behaviour of the decarboxylated aristolochic acids is also discussed. A mechanism is proposed for the favourable loss of CH 2O in the 8-methoxy isomer.

The fragmentations of substituted cinnamic acids after electron impact

AbstractThe fragmentations of a number of cinnamic acids substituted at the phenyl ring have been studied with the aid of 70 eV mass spectra and mass analysed ion kinetic energy spectra. Evidence is presented that the formation of [C9H7O2]+ ions occurs by intramolecular aromatic substitution reactions. A mechanism is proposed for the energetically favourable loss of the substituents from meta and para positions of the phenyl ring. The analytical use of intramolecular aromatic substitution reactions is briefly discussed.

Formation of 2-methylbenzopyrylium ions from the molecular ions of benzalacetones

It can be shown by the method of metastable ion characteristics that different C 10H 9O + ions do not rearrange to a common reactive form. The metastable ion characteristics of C 10H 9O + ions can therefore be used to determine the structure of the ion. Using these methods, metastable C 10H 9O + derived from the molecular ions of substituted benzalacetones 1 are shown to correspond to 2-methyl-benzopyrylium ions 3. This confirms that the loss of a hydrogen atom or a substituent from the phenyl group of the molecular ions of 1 occurs by an intramolecular aromatic substitution reaction. 3 is formed not only from ortho-substituted benzalacetones, but also from the meta- and para-substituted derivatives. In the latter cases a sufficiently long-lived intermediate must be formed, which reacts to produce 3 by hydrogen migrations prior to elimination of the substituent. This reaction model is corroborated by a calculation of the dependence of ion abundances on the electron energy, and of the frequency factors of the gas phase reactions of the three isomeric chlorobenzalacetones.

Mass Spectrometry of Some Substituted 2-Benzylidenecyclohexanones and 2,6-bis-Benzylidenecyclohexanones

The mass spectra of a series of some substituted 2-benzylidenecyclohexanones and a series of substituted 2,6-bis-benzylidenecyclohexanones have been determined at 70 eV. The major fragmentation pathways include an intramolecular aromatic substitution reaction leading to the loss of an ortho-substituent with the formation of a stable benzopyrylium ion, loss of carbon monoxide and ethylene from the parent ion and also further ions derived from subsequent cleavages of the cyclohexanone ring. The structural and electronic factors involved in the aromatic substitution reaction were examined by comparing the M – H/M and M – Cl/M ratios determined from the spectra of the various substrates.