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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165988Generated: November 2, 2026

Benzoyl chloride → HCID 15615679, compound

https://huagongshe.com/reaction/2165988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantCyclohexanecarboxylic acid, 3,5-dioxo-, ethyl esterHCID 11252382—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 15615679HCID 15615679—

Reaction Steps

7.75 g (55.1 mmol) Benzoyl chloride was added dropwise to 10.00 g (54.3 mmol) ethyl 3,5-dioxocyclohexanecarboxylate, dissolved in 100 ml dichloromethane and 15 ml triethylamine, at 10° C. The mixture was stirred for 3 hours at room temperature, poured into ice, separated, the organic phase shaken with 1N hydrochloric acid, saturated sodium bicarbonate and water, dried (magnesium sulphate) and concentrated. The ethyl 3-benzoyloxy-5-oxo-3-cyclohexenecarboxylate, so obtained, was dissolved in 75 ml acetonitrile and after addition of 15 ml triethylamine and 1.5 ml 2-hydroxyisobutyronitrile, was stirred at 24 hours at room temperature. The mixture was taken up in 100 ml diethyl ether and extracted with 100 ml 2N hydrochloric acid and then twice with, each time, 50 ml 5% potassium carbonate solution. After covering the aqueous phase with a layer of 100 ml diethyl ether, it was acidified with 4N hydrochloric acid until it was pH 3, separated, washed with water, dried (magnesium sulphate) and evaporated on a rotary evaporator. It was purified by recrystallising from hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04943310
Source datasetuspto-grants-1990_07
ORD IDord-af2675a4e17f4d40ba9df1a2ee9de649
Source noteuspto-grants-1990_07