HRID1708625

反应详情

EQUATION

反应方程式

HRID 1708625 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 20.0 grams (70 mmol) of 4-hydroxy-1-octyloxy-2,2,6,6-tetramethylpiperidine (prepared in Example 5), 1.68 gram (70 mmol) of sodium hydride, 2 ml of dimethyl sulfoxide, and 150 ml of tetrahydrofuran is heated at reflux for three hours. The reaction mixture is cooled to room temperature, and a solution of 6.5 grams (70 mmol) of epichlorohydrin in 50 ml of tetrahydrofuran is added over a 5-minute period. The reaction mixture is stirred sixteen hours at room temperature and then partitioned between ether and water. The aqueous layer is extracted with ether and the combined ether solutions are dried over anhydrous magnesium sulfate before concentrating to yield an oil. Purification by flash chromatography (4:1 hexane:ethyl acetate) affords 3.9 grams (16% yield) of the title compound as a colorless oil.

WORKUP

后处理

  1. temperatureis heated
  2. temperatureat reflux for three hours
  3. custompartitioned between ether and water
  4. extractionThe aqueous layer is extracted with ether
  5. dry with materialthe combined ether solutions are dried over anhydrous magnesium sulfate
  6. concentrationbefore concentrating
  7. customto yield an oil
  8. customPurification by flash chromatography (4:1 hexane:ethyl acetate)