posted on 2024-11-25, 08:29authored byMark H.
S. Troftgruben, Isabella Oldenburg, Alyssa M. Pama, Bryce Igawa, Salvatore Deguara, Maya Shields, Neil K. Viswanathan, Joshua X. Silverio, Cameron Gleason, Justin Shan-Min Wang, Jordan S. Ford, Horacio Lazaro, Scott Eagon
A microwave-based method for the acylation of alcohols,
phenols,
and thiols has been developed without the need of a catalyst or base
additives. The reaction is far more rapid than previously reported
acylation methods, tolerates a wide variety of functional groups,
and provides easy isolation of products in excellent yields without
the need for chromatography. Most products can be isolated directly
via evaporation under reduced pressure or by pouring the reaction
mixture into water and filtering.