HRID2387310

反应详情

EQUATION

反应方程式

HRID 2387310 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
40 °C

PROCEDURE

实验过程

A solution of 3-(5,5-dimethyl-3-prop-2-ynyl-3-trifluoromethyl-1,3,4,5-tetrahydrobenzo[c]oxepin-1-yloxy)propan-1-ol (15.0 g) in THF (150 mL) was treated with 1M aqueous HCl (75 mL) and heated at 40° C. for 16 hours. The volatiles were then removed in vacuo and the aqueous layer extracted with ethyl acetate (300 mL), washed with two 100 mL portions of saturated aqueous sodium bicarbonate solution, dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude was purified by flash chromatography (300 g SiO2, hexanes to 4:1 hexanes:EtOAc) to give 5,5-dimethyl-3-prop-2-ynyl-3-trifluoromethyl-1,3,4,5-tetrahydrobenzo[c]oxepin-1-ol (5.75 g, 46%) as a 1:1 mixture of lactol and aldehyde by NMR. The mixture was used without further purification in the next transformation.

WORKUP

后处理

  1. customThe volatiles were then removed in vacuo
  2. extractionthe aqueous layer extracted with ethyl acetate (300 mL)
  3. washwashed with two 100 mL portions of saturated aqueous sodium bicarbonate solution
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe crude was purified by flash chromatography (300 g SiO2, hexanes to 4:1 hexanes:EtOAc)