HRID276113

反应详情

EQUATION

反应方程式

HRID 276113 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

Combine 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine (0.14 g, 0.34 mmol), (L)-phenylalanine t-butyl ester hydrochloride salt (0.174 g, 68 mmol), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.13 g, 0.67 mmol) in dichloromethane (5 mL). Add N-methylmorpholine (0.1 mL, 1.01 mmol) and hydroxybenzotriazole (0.091 g, 0.67 mmol). After 3 hours, after 1 hour, partition the reaction mixture between methyl t-butyl ether and an aqueous 5% sulfuric acid solution. Separate the layers, extract the organic layer with a saturated sodium bicarbonate solution and then brine. Dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting sequentially with 3/1 hexane/ethyl acetate and then 1/1 hexane/ethyl acetate to give the title compound: Rf=0.45 (silica gel, 1/1 ethyl acetate/hexane).

WORKUP

后处理

  1. waitafter 1 hour
  2. custompartition the reaction mixture between methyl t-butyl ether
  3. customSeparate the layers
  4. extractionextract the organic layer with a saturated sodium bicarbonate solution
  5. dry with materialDry over Na2SO4
  6. filtrationfilter
  7. customevaporate in vacuo
  8. customto give a residue