作者:C. Combellas、C. Suba、A. Thiébault
DOI:10.1016/s0040-4039(00)77067-5
日期:1994.7
regioselectively from 2-tert-butyl-1-napthol by an electro-induced SRN1 reaction in liquid ammonia. The reaction is illustrated with different aryl chlorides as starting compounds (aryl= pyridyl, quinolinyl, phenylpyridine); the yields are between 60 and 85%. The tert-butyl substituent can be further eliminated by a trans-alkylation reaction.
通过在液体氨中的电诱导的S RN 1反应从2-叔丁基-1-萘醇区域选择性地获得4-芳基-2-叔丁基-1-萘酚。用不同的芳基氯化物作为起始化合物(芳基=吡啶基,喹啉基,苯基吡啶)说明了该反应;收率在60%至85%之间。叔丁基取代基可以通过烷基转移反应进一步消除。