摘要
利用三甲基氯硅烷作为氯源,在二乙酸碘苯促进下,以芳基酮衍生的烯醇硅醚作为底物,合成了一系列α-氯代芳基酮.该方法反应条件温和,以中等至较好收率得到氯代芳基酮.若使用三甲基溴硅烷作为溴源,该方法还能用来制备α-溴代芳基酮.
A series of α-chloroketones were obtained from silyl enol ethers of aryl ketones using trimethylchlorosilane as chlorine source and diacetoxyiodobenzene as promoter. The reaction occurs under mild condition yielding the product in moderate to good yields, and has the potential possibility for the synthesis of α-bromoketone by using trimethyl bromosilane as bromine source.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2016年第5期1028-1033,共6页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(Nos.21362033
21502154)资助项目~~
关键词
α-氯代
二乙酸碘苯
烯醇硅醚
芳基酮
α-溴代芳基酮
α-chlorination
diacetoxyiodobenzene
silyl enol ether
aryl ketone
α-bromoaryl ketone