HRID1922

反应详情

EQUATION

反应方程式

HRID 1922 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

N-(t-Butoxycarbonyl)-O-benzyl-D-serine (600 mg; 2.03 mmol) was dissolved in dry methylene chloride (5 ml), allyl alcohol (152 μl; 2.23 mmol) and DMAP (25 mg; 0.20 mmol) added and finally EDC (428.5 mg; 2.24 mmol) added to the acid. The reaction mixture was stirred at room temperature for 2.5 h and the resulting homogeneous solution quenched with water and extracted with methylene chloride. The methylene chloride layer was washed with 5% aqueous citric acid then 10% aqueous sodium carbonate solution. The methylene chloride layer was dried over anhydrous magnesium sulfate powder, filtered and evaporated under reduced pressure to give an oil. Chromatography of the oil using ethyl acetate and hexanes 1:2 v/v afforded the product (408 mg; 60%) as a pale yellow gum. FAB-MS:- Calculated for C36H33N5 335.1; found 336.1 (M+1).

WORKUP

后处理

  1. customthe resulting homogeneous solution quenched with water
  2. extractionextracted with methylene chloride
  3. washThe methylene chloride layer was washed with 5% aqueous citric acid
  4. dry with materialThe methylene chloride layer was dried over anhydrous magnesium sulfate powder
  5. filtrationfiltered
  6. customevaporated under reduced pressure
  7. customto give an oil
  8. customafforded the product (408 mg; 60%) as a pale yellow gum