有机化学 ›› 1987, Vol. 7 ›› Issue (5): 350-353. 上一篇    下一篇

研究论文

不对称诱导II.相转移催化下苯甲醛与氯仿、手性胺的反应

施耀曾;潘友;吕龙;陆婉芳;胡宏纹   

  1. 南京大学化学系
  • 发布日期:1987-10-25

Asymmetric induction II. phase transfer catalyzed reaction of benzaldehyde with chloroform and chiral amines

SHI YAOZENG;PAN YOU;LU LONG;LU WANFANG;HU HONGWEN   

  • Published:1987-10-25

用溴化四正丁基铵作为相转移催化剂,苯甲醛、氯仿、α-苯基乙胺(1a~c)和固体氢氧化钾在-5~0℃于无水无腈中反应。反应产物2a~c经水解、氢解得到相应的光学活性苯甘氨酸(4a~c)。由1-苯基-2,2,2-三氯乙醇与1a反应也可制得2a,并对反应机理进行了讨论。

关键词: 苯乙胺 P, 水解, 苯 P, 氯仿, 相转移催化, 苯甲醛, 甘氨酸, 手征性, 氢解, 诱导效应, 不对称反应

Reaction of benzaldehyde, chloroform, RNH2 (R = DL-PhCHMe, (R)-(+)-PhCHMe, (S)-(-)-PhCHMe), and solid potassium hydroxide was carried out in anhydrous acetonitrile at -5-0癈, with tetra-Bu ammonium bromide as phase transfer catalyst. The reaction products I were hydrolyzed and hydrogenolyzed to yield the corresponding optically active phenylglycine. I (R = DL-CHPhMe) could be also obtained by reaction of 1-phenyl-2,2,2-trichloroethanol with DL-PhCHMeNH2. The reaction mechanism was discussed.

Key words: PHENYLETHYLAMINE P, HYDROLYSIS, BENZENE P, CHLOROFORM, PHASE TRANSFER CATALYSIS, BENZALDEHYDE, GLYCINE, CHIRALITY, HYDROGENOLYSIS, INDUCTIVE EFFECT

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