Abstract

AbstractThe direct employment of benzylic and allylic alcohols as N‐alkylating agents provides a useful synthetic route for amine derivatives by avoiding the preactivation of the hydroxy groups of alcohols. Herein we report a novel by‐product‐catalyzed three‐component synthesis of amine derivatives from readily available benzylic and allylic alcohols, acyl chlorides (chloroformates or sulfonyl chlorides), and hexamethyldisilazane (HMDS). In the absence of external catalysts and additives, a range of benzylic and allylic alcohols have been transformed into the corresponding N‐alkyl amides (carbamates or sulfonamides) in good to excellent yields. Furthermore, by‐product TMSCl and its decomposition into HCl have been found to be responsible for promoting the three‐component reaction of benzylic (or allylic) alcohols with acyl chlorides (chloroformates or sulfonyl chlorides) and HMDS.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)

Full Text
Paper version not known

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 call

Disclaimer: 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.