反应 #452446

反应方程式

Ammonium chloride

ammonium hydroxide

3,7-Dimethyl-1,6-octadien-3-yl 3-oxo-butyrate

HCl

Calcium hydroxide

Heptanoyl chloride

→

desired compound

3,7-dimethyl-1,6-octadien-3-yl 3-(hexyl)-3-oxo-propionate

溶剂

water

dichloromethane

methyl ethyl ketone

dichloromethane

dichloromethane

反应条件

后处理

1. 1
   其他fitted with an internal thermometer, addition funnel, condenser and argon inlet
2. 2
   其他between 35-40° C
3. 3
   workup.ADDITIONis added to the flask
4. 4
   workup.WAITAfter 20 min
5. 5
   workup.WAITAfter 1 h
6. 6
   workup.WAITAfter 1 h
7. 7
   其他The layers are separated
8. 8
   萃取the aqueous phase extracted with 100 mL of dichloromethane
9. 9
   洗涤The combine organic layers are washed with saturated NaHCO3 solution, water
10. 10
    干燥dried over MgSO4
11. 11
    过滤filtered
12. 12
    浓缩concentrated by rotary evaporation
13. 13
    其他purified by flash chromatography

实验过程

3,7-Dimethyl-1,6-octadien-3-yl 3-oxo-butyrate (30.00 g, 0.126 mol), dichloromethane (50 mL) and methyl ethyl ketone (10 mL) are combined in a 500 mL three-necked round-bottomed flask fitted with an internal thermometer, addition funnel, condenser and argon inlet. Calcium hydroxide (9.80 g, 0.132 mol, powdered) is added to the flask and the slurry stirs for 1 h. Heptanoyl chloride (17.84 g, 0.120 mol) in 10 ml of dichloromethane is added over 15 min so as to keep the reaction temperature between 35-40° C. The reaction continues to stir at 35-40° C. for 2 h. Ammonium chloride (7.06 g, 0.132 mol) dissolved in 20 mL of water is added to the flask. After 20 min, concentrated ammonium hydroxide is added to the mixture to adjust the pH to ~9.0. After 1 h, 20% HCl solution is added to drop the pH to ~1.0. After 1 h, the mixture is poured into 300 mL of dichloromethane. The layers are separated and the aqueous phase extracted with 100 mL of dichloromethane. The combine organic layers are washed with saturated NaHCO3 solution, water, dried over MgSO4, filtered, concentrated by rotary evaporation and purified by flash chromatography to yield the desired compound. Structure is confirmed my 1H and 13C NMR.

来源