HRID1952545

反应详情

EQUATION

反应方程式

HRID 1952545 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
75 °C

PROCEDURE

实验过程

A mixture of methanesulfonic acid 3-(3-methoxy-phenyl)-propyl ester (1.20 g, 4.912 mmol), 4-Methyl-2-oxo-2,3-dihydro-thiazole-5-carboxylic acid ethyl ester (0.960 g, 5.128 mmol) and cesium carbonate (3.2 hm, 9.82 mmol) in anhydrous DMF was heated to oil bath at 75° C. for 2.5 h. The reaction mixture was cooled, concentrated and diluted with water (50 mL) and extracted with EtOAc (3×50 mL). The organic layers were washed with 2N HCl (30 mL), water ((30 mL), brine (30 mL), dried over magnesium sulphate, filtered and concentrated to give a brown oil. The crude product is purified by flash column chromatography (10%-30% EtOAc in hexane) to give 2-[3-(3-Methoxy-phenyl)-propoxy]-4-methyl-thiazole-5-carboxylic acid ethyl ester (0.84 g, 51%) as a yellow oil. MS m/e 336.4 (M+H+).

WORKUP

后处理

  1. temperatureThe reaction mixture was cooled
  2. concentrationconcentrated
  3. additiondiluted with water (50 mL)
  4. extractionextracted with EtOAc (3×50 mL)
  5. washThe organic layers were washed with 2N HCl (30 mL), water ((30 mL), brine (30 mL)
  6. dry with materialdried over magnesium sulphate
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customto give a brown oil
  10. customThe crude product is purified by flash column chromatography (10%-30% EtOAc in hexane)