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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261589Generated: October 25, 2026

Potassium Hydroxide → 3-Chloro-4-cyclohexylpropiolic acid

https://huagongshe.com/reaction/261589

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 numberUS04166133
Source datasetuspto-grants-1979_08
ORD IDord-0b19a350062c4f358df6b9a30136811a
Source noteuspto-grants-1979_08