Abstract
An environmentally benign and practical preparation method for the Vilsmeier-Haack reagent (VH) has been developed by using phthaloyl dichloride with DMF in toluene or 2-chlorotoluene. Phthalic anhydride as the byproduct was recovered in high yield by simple filtration. Some aromatic acids have been transformed into the corresponding acid chlorides in good yields by employing the isolated VH. Treatment of primary or secondary alcohols with VH gave alkyl formates or alkyl chlorides by depending on the reaction conditions.
Highlights
We have recently reported a new method for the preparation of the Vilsmeier-Haack reagent (VH) [1,2,3,4,5,6]
We show some examples of synthesis of acid chlorides from carboxylic acids, alkyl formates from alcohols, and alkyl chlorides from alcohols using the OPC-VH reagent prepared through the new method
We first examined the use of toluene as a solvent for the preparation of the OPC-VH reagent
Summary
We have recently reported a new method for the preparation of the Vilsmeier-Haack reagent (VH) [1,2,3,4,5,6]. Our method obviates the use of toxic reagents such as phosgene, thionyl chloride, or phosphoryl chloride, which are used in the conventional method It involves synthesis of VH reagent from N,N-dimethylformamide (DMF) and phthaloyl dichloride (OPC) in 1,4-dioxane (Scheme 1) [7]. We show some examples of synthesis of acid chlorides from carboxylic acids, alkyl formates from alcohols, and alkyl chlorides from alcohols using the OPC-VH reagent prepared through the new method. Products of these syntheses do have not contaminants such as sulfur or Scheme 1.
Sign-in/Register to view highlights & summary Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
