A series of C-2 substituted 3-methylcyclohex-2-enones has been prepared using the Hagemann ester route. A new synthesis of these compounds has been developed which involves the alkylation of the N,N-diethylaminoethyl ether of 1-hydroxy-5-methylcyclohexa-1,5-diene. The cyclohexenones have been converted into the corresponding α,β-epoxyketones using alkaline hydrogen peroxide.
使用哈格曼酯途径已经制备了一系列的C-2取代的3-甲基环己-2-烯酮。已经开发了这些化合物的新合成方法,其涉及1-羟基-5-甲基环己-1,5-二烯的N,N-
二乙基氨基
乙基醚的烷基化。使用碱性
过氧化氢已将
环己酮转化为相应的α,β-环氧酮。