作者:Hiroshi Kimoto、Hiroshige Muramatsu、Kan Inukai
DOI:10.1246/bcsj.49.1642
日期:1976.6
1,1,2,3,3,3-hexafluoropropyl ketone(I) and 2,2,3-trifluoro-3-(trifluoromethyl)indanone(II) were synthesized by the radical-addition reaction of benzaldehyde to hexafluoropropene. The reduction with NaBH4 and the Grignard reaction with methylmagnesium iodide of these ketones gave the corresponding secondary and tertiary alcohols respectively. A Clemmensen reduction, alkaline hydrolyses, and reactions
通过苯甲醛与六氟丙烯的自由基加成反应合成了苯基1,1,2,3,3,3-六氟丙基酮(I)和2,2,3-三氟-3-(三氟甲基)茚满酮(II)。这些酮用 NaBH4 还原,并与这些酮的碘化甲基镁进行格氏反应,分别得到相应的仲醇和叔醇。还进行了克莱门森还原、碱性水解以及与羟胺和重氮甲烷的反应。