Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289413Generated: October 29, 2026

Hydrochloric Acid → 3,7-Dimethyl-1,6-octadien-3-yl 3-(hexyl)-3-oxo-propionate

https://huagongshe.com/reaction/2289413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium HydroxideHCID 14923—
ReactantHeptanoyl chlorideHCID 17313—
ReactantAmmonium ChlorideHCID 25517—
ReactantCalcium HydroxideHCID 6093208—
ReactantLinalyl acetoacetateHCID 11791251—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventMethyl Ethyl KetoneHCID 6569—
Product3,7-Dimethyl-1,6-octadien-3-yl 3-(hexyl)-3-oxo-propionateHCID 21260236—

Reaction Conditions

Temperature37.5 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093691
Source datasetuspto-grants-2000_07
ORD IDord-5a600e776fff476d864a514a6aa2e25a
Source noteuspto-grants-2000_07