反应 #58349

反应方程式

methanol

(±)-3,4-bis-cyclopropylmethoxy-N-[(3RS,4RS)-4-(3,4-dimethoxyphenyl)-7-oxabicyclo[4.1.0]-hept-3-yl]benzamide

compound E1

(±)-3,4-bis-cyclopropylmethoxy-N-[(3RS,4RS)-4-(3,4-dimethoxyphenyl)-7-oxabicyclo[4.1.0]-hept-3-yl]benzamide

water

sodium borohydride

→

title compound

收率 68.2%

(±)-3,4-Bis-cyclopropylmethoxy-N-[(1RS,2RS,5RS)-2-(3,4-dimethoxyphenyl)-5-hydroxycyclohexyl]benzamide

收率 68.2%

溶剂

tert-butanol

ethyl acetate

反应条件

后处理

1. 1
   温度the reaction mixture is heated to boiling
2. 2
   温度the reaction mixture is cooled
3. 3
   其他The organic phase is dried
4. 4
   浓缩concentrated
5. 5
   其他the residue is chromatographed on silica gel using
6. 6
   workup.ADDITIONa mixture of petroleum ether/ethyl acetate in the ratio 1/2

实验过程

16.5 g of (±)-3,4-bis-cyclopropylmethoxy-N-[(3RS,4RS)-4-(3,4-dimethoxyphenyl)-7-oxabicyclo[4.1.0]-hept-3-yl]benzamide (compound E1) are dissolved in 500 ml of tert-butanol, 5.0 g of sodium borohydride are added and the reaction mixture is heated to boiling. After slow addition of 70 ml of methanol, the reaction mixture is cooled and treated with 200 ml of water and 150 ml of ethyl acetate. The organic phase is dried using sodium sulfate, concentrated and the residue is chromatographed on silica gel using a mixture of petroleum ether/ethyl acetate in the ratio 1/2. 11.3 g of the title compound are obtained.

来源