HRID67901

反应详情

EQUATION

反应方程式

HRID 67901 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

N,N'-Dicyclohexylcarbodiimide (10.3 g, 50 mmol) in methylene chloride (80 ml) was added to 2-acetylthio-3-methoxybenzoic acid (11.3 g, 50 mmol) and N-cyclopentylglycine t-butyl ester (10.0 g, 50 mmol) in methylene chloride (300 ml) at 0°-5° C. Overnight stirring was followed by filtration and washing of the filtrate with dilute hydrochloric acid, sodium bicarbonate solution and brine. Dryng and concentration gave a gum which was dissolved in acetonitrile (65 ml), combined with sodium iodide (11.2 g, 75 mmol) and heated to 40°-50° C. Chlorotrimethylsilane (8.1 g, 75 mmol) was introduced and the mixture was heated for 30 minutes, then quenched with water. The organic phase was washed with water, aqueous sodium thiosulfate and brine then concentrated. Aqueous sodium bicarbonate was added to the residue and the resulting solution was washed with methylene chloride and ether, then acidified and extracted with ethyl acetate. The organic portion was dried and concentrated and the residue passed through a silica gel column to provide the amorphous product.

WORKUP

后处理

  1. filtrationwas followed by filtration
  2. washwashing of the filtrate with dilute hydrochloric acid, sodium bicarbonate solution and brine
  3. concentrationDryng and concentration
  4. customgave a gum which
  5. temperatureheated to 40°-50° C
  6. temperaturethe mixture was heated for 30 minutes
  7. customquenched with water
  8. washThe organic phase was washed with water, aqueous sodium thiosulfate and brine
  9. concentrationthen concentrated
  10. additionAqueous sodium bicarbonate was added to the residue
  11. washthe resulting solution was washed with methylene chloride and ether
  12. extractionextracted with ethyl acetate
  13. customThe organic portion was dried
  14. concentrationconcentrated
  15. customto provide the amorphous product