HRID431820

反应详情

EQUATION

反应方程式

HRID 431820 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
2 °C

PROCEDURE

实验过程

A solution of 76 g (0.68 mol) potassium-tert.-butylate in 1.5 l DMF was cooled (−3° C.) and treated slowly (1.5 h) with 202 g (0.73 mol) triphenylmethanethiol in 0.8 l DMF (at max 1° C.). After 2.5 h at 0° C., a solution of 161 g (0.61 mol) of (2S,4S)-4-Chloro-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester in 0.35 l DMF was added. The reaction was stirred over night at 2° C., evaporated, dissolved in 1.5 l EtOAc, poured into 2.7 l aqueous saturated NH4Cl solution and extracted with EtOAc (2×). The organic phase was washed with aqueous saturated NaHCO3, dried over Na2SO4 and evaporated. Colum chromatographyon silica gel with hexane/EtOAc (95:5 to 7:3) gave 268 g (87%) (2S,4R)-4-Tritylsulfanyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester, MS: 504 (MH30 ).

WORKUP

后处理

  1. customevaporated
  2. dissolutiondissolved in 1.5 l EtOAc
  3. additionpoured into 2.7 l aqueous saturated NH4Cl solution
  4. extractionextracted with EtOAc (2×)
  5. washThe organic phase was washed with aqueous saturated NaHCO3
  6. dry with materialdried over Na2SO4
  7. customevaporated