82259-92-5Relevant articles and documents
General and efficient transesterification of β-keto esters with various alcohols using Et3N as a br?nsted base additive
Mhasni, Olfa,Erray, Imen,Rezgui, Farhat
, p. 3320 - 3327 (2014)
Transesterification of β-keto esters with a wide variety of allyl, benzyl, propargyl, and alkyl alcohols using, for the first time, commercially available and inexpensive Et3N as a Br?nsted base additive, is efficiently performed in toluene at reflux. The corresponding esters are exclusively obtained in 57-98% yields with no trace amounts of γ,δ-ketones, usually expected from the decarboxylative Carroll rearrangement.
AgOTf-catalyzed transesterification of β-keto esters
Das, Rima,Chakraborty, Debashis
experimental part, p. 140 - 144 (2012/05/20)
AgOTf proved to be an effective catalyst for the transesterification of β-keto esters with primary, secondary and tertiary alcohols. The products were obtained in high yield within a reasonable reaction time period. The kinetics of the transesterification reaction were also studied and the reaction was found to follow second-order kinetics. Copyright