反応 #452446

反応方程式

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

溶媒

water

dichloromethane

methyl ethyl ketone

dichloromethane

dichloromethane

反応条件

後処理

1. 1
   その他fitted with an internal thermometer, addition funnel, condenser and argon inlet
2. 2
   その他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
   その他The layers are separated
8. 8
   抽出the aqueous phase extracted with 100 mL of dichloromethane
9. 9
   洗浄The combine organic layers are washed with saturated NaHCO3 solution, water
10. 10
    乾燥dried over MgSO4
11. 11
    ろ過filtered
12. 12
    濃縮concentrated by rotary evaporation
13. 13
    その他purified by flash chromatography

実験手順

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.

出典