The Wittig reaction carried out in a slighty hydrated solid-liquid media constituted by a solid alkaline hydroxyde and an organic phase which includes the phosphonium salt and the aldehyde leads easily to the corresponding alkene with very good yields specially with furanic aldehydes. The ylide formation at the interface appears as the most important step of this condensation.
在由固体碱性羟基和包括phase盐和醛的有机相组成的略微
水合的固液介质中进行的Wittig反应易于以非常好的收率产生相应的烯烃,特别是
呋喃醛。界面处的叶立德形成似乎是这种缩合的最重要步骤。