HRID1274263

反应详情

EQUATION

反应方程式

HRID 1274263 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To a suspension of 1-(4-methylphenyl)cyclopentane carboxylic acid (3.00 g, 14.7 mmol) in dichloromethane (50 ml,) at 0° C. was added oxalyl chloride (1.54 mL, 17.4 mmol) and DMF (2 drops). The mixture was stirred at 0° C. for 1 hour, and at rt for 2 hours. The solution was concentrated, diluted with THF (40 mL), and cooled to 0° C. Potassium t butoxide (1.80 g, 16.2 mmol) in THF (20 mL) was slowly added, and the mixture was stirred overnight at rt. Additional potassium t butoxide (0.660 g, 5.88 mmol) was added. After 20 minutes the solution was concentrated to dryness, and taken up in ethyl acetate. The organic phase was washed with 10% citric acid, saturated NaHCO3 and brine, dried (MgSO4), and concentrated. Flash column chromatography (10% ethyl acetate/hexane) gave 1-(4-methylphenyl)cyclopentane carboxylic acid t butyl ester (3.27 g, 87%).

WORKUP

后处理

  1. waitat rt for 2 hours
  2. concentrationThe solution was concentrated
  3. additiondiluted with THF (40 mL)
  4. temperaturecooled to 0° C
  5. stirringthe mixture was stirred overnight at rt
  6. concentrationAfter 20 minutes the solution was concentrated to dryness
  7. washThe organic phase was washed with 10% citric acid, saturated NaHCO3 and brine
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated