HRID131772

反应详情

EQUATION

反应方程式

HRID 131772 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of (±)-N,N-diisopropyl-3-(2-methoxy-5-methoxycarbonylphenyl)-3-phenylpropionamide (0.79 g, 2.0 mmol) in 20 ml of tetrahydrofuran was cooled to 5° C. and then treated with 2.5 ml of 1M LiAlH4/THF. After stirring at room temperature for 18 hrs. finely powdered aluminium chloride (0.3 g) was added and stirring was continued for additional 4 hrs. The reaction was quenched at 5° C. by the dropwise addition of water followed by aqueous sodium hydroxide solution. The mixture was diluted with diethyl ether (150 ml) and the organic phase was washed with half saturated brine, dried (sodium sulphate), and evaporated to dryness to give the title compound as a solid off-white foam. Tlc (2) 0.16, m.p. 48-51° C. A portion of the material was converted into the hydrochloride (ethereal hydrochloric acid), m.p. 186-189° C. (dec.).

WORKUP

后处理

  1. stirringstirring
  2. waitwas continued for additional 4 hrs
  3. customThe reaction was quenched at 5° C. by the dropwise addition of water
  4. additionThe mixture was diluted with diethyl ether (150 ml)
  5. washthe organic phase was washed with half saturated brine
  6. dry with materialdried (sodium sulphate)
  7. customevaporated to dryness