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作 者:任正红[1] 李晟[1] 张兴花[1] 范莉[1] 周光明[1] 杨大成[1]
出 处:《有机化学》2013年第5期1047-1056,共10页Chinese Journal of Organic Chemistry
基 金:重庆市科技攻关计划(Nos.2011AB5001;2011AC1053);国家自然科学基金(No.21172181);中央高校基本科研业务费专项资金(No.XDJK2010C067)资助项目~~
摘 要:以对甲基苯乙酮、芳香醛和乙腈为主要原料,通过三氟乙酸催化的改进的Dakin-West反应,顺利得到28个N-[3-(4-甲基苯基)-3-氧代-1-芳基丙基]乙酰胺,最高收率可达95%.18个新化合物的结构经1H NMR,13C NMR和HRMS证实.结构测试发现,羟基苯甲醛参与Dakin-West反应后得到的全部是羟基乙酰化的产物.作者首次证实,羟基苯甲醛参与的Dakin-West反应不是串联反应,而是羟基苯甲醛首先经TFA催化转化为乙酰氧基苯甲醛,然后参与Dakin-West反应,最终生成羟基乙酰化产物.通过碱性水解,可以选择性高收率地制备对应的羟基化β-乙酰氨基酮,同时也反证了羟基乙酰化产物的存在.该研究扩展了TFA催化的Dakin-West反应,为β-乙酰氨基酮的合成提供了新的方法.The synthesis of a series ofN-[3-(4-methylphenyl)-3-oxo-1-arylpropyl]acetamides using trifluoroacetic acid (TFA) as the catalyst was reported in this paper. It was achieved by a modified Dakin-West reaction using 4-methylacetophenone, aromatic aldehydes and acetonitrile as starting materials, The highest yield was up to 95% among the twenty eight target com- pounds synthesized. All the new compounds were characterized by 1H NMR, 13C NMR and HRMS spectra. This one-pot reac- tion offered several advantages including small catalyst loading (0.3 mol%), moderate reaction temperatures (28-35℃) and simple post treatment procedure. A reaction mechanism was for the first time established, in which hydroxybenzaldehyde was first catalytically converted into corresponding acetoxybenzaldehyde prior to be involved in the subsequent Dakin-West reac- tion that eventually led to hydroxyl acetylated target compounds. The resultant hydroxyl acetylated β-acetamido ketones were selectively deacetylated in LiOH to produce the corresponding hydroxyl products with excellent yields. The current work fur- ther demonstrated that TFA was an efficient catalyst for Dakin-West reaction involving arylalkyl ketones, aromatic aldehydes and acetonitrile, which expanded significantly the scope of the substrates and provided a new synthetic route to β-acetamido ketones.
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