HRID1395629

反应详情

EQUATION

反应方程式

HRID 1395629 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A solution of 2 g(8 mmoles) of optically pure (R)-(+)-3,4-dihydro-6-hydroxy-2,5,7,8-tetramethyl-2H-1-benzopyran-2-carboxylic acid; [α]D25 + 65.84° (c 1.18, C2H5OH) and 0.1 g of p-toluenesulfonic acid monohydrate in 40 ml of methanol was stirred and refluxed for 3.75 hr. After cooling, the solution was diluted with water and worked-up with ether in the usual manner (the ether extracts were additionally washed with saturated aqueous sodium bicarbonate solution) giving 2g (94.7%) of (R)-(+)-3,4-dihydro-6-hydroxy-2,5,7,8-tetramethyl-2H-1-benzopyran-2-carboxylic acid methyl ester as a colorless solid, mp 132°-134.5°; [α]D25 +61.4° (c 4.91, CH3OH). The analytical specimen was obtained by recrystallization of a sample from aqueous methanol as a colorless solid, mp 133.5°-135°; [α]D25 +61.85° (c 5.07, CH3OH).

WORKUP

后处理

  1. temperaturerefluxed for 3.75 hr
  2. temperatureAfter cooling
  3. washwere additionally washed with saturated aqueous sodium bicarbonate solution)