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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576648Generated: November 2, 2026

Potassium Hydroxide → 3-Chloro-4-cyclohexylpropiolic acid

https://huagongshe.com/reaction/1576648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl alpha,beta-dibromo-beta-(3-chloro-4-cyclohexyl)propionateHCID 57052243—
Product3-Chloro-4-cyclohexylpropiolic acidHCID 70542015—

Reaction Steps

Powdered ethyl α,β-dibromo-β-(3-chloro-4-cyclohexyl)propionate (33.0 g.) is added portion-wise to 20% ethanolic potassium hydroxide (135 ml) at room temperature. The mixture is refluxed on a steam bath for 6 hours. The alcohol is evaporated and the residue is dissolved in water and covered with ether and is acidified with cold, dilute hydrochloric acid. The ether layer is washed with water, saline, and dried over sodium sulfate. The ether is removed to give a residue which is triturated with carbon tetrachloride. Recrystallization is carried out from acetic acid-water. This material is digested and triturated with boiling carbon tetrachloride to give 3-chloro-4-cyclohexylpropiolic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03981932
Source datasetuspto-grants-1976_09
ORD IDord-f4dd8064affe4b56bb1f2a437d8f658d
Source noteuspto-grants-1976_09