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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426812Generated: October 26, 2026

Ammonia → 3-Chloro-4-cyclohexylethynylbenzene

https://huagongshe.com/reaction/426812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium amideHCID 24533—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant3-Chloro-4-cyclohexylacetophenoneHCID 56975890—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product3-Chloro-4-cyclohexylethynylbenzeneHCID 57286755—

Reaction Steps

3-Chloro-4-cyclohexylacetophenone (0.25 moles) and phosphorus pentachloride (0.31 moles) are placed in a 3-necked flask equipped with a mechanical stirrer, a condenser connected to a nitrogen inlet, and a thermometer. The mixture is stirred at 33°-35° C. for 3 days. The cooled reaction mixture is poured onto 800 g. of ice and extracted with 3×500 ml. of ether. The ether fraction is washed with 2×100 ml water 4×100 ml of 5% sodium hydroxide, 3×=ml water, 2×50 ml of saturated saline and dried over sodium sulfate. The ether is removed to give the chlorinated intermediate. The intermediate is dissolved in anhydrous THF (200 ml) and is added dropwise to a freshly prepared solution of sodamide in liquid ammonia, using a dry-ice condenser. The reaction mixture is allowed to stir at room temperature overnight; then, it is poured into 50 ml of water and 500 ml of ether. The ether fraction is washed with 3×50 ml water and 50 ml of saturated saline and is dried over sodium sulfate. Removal of solvent gives a residue which is distilled to give 3-chloro-4-cyclohexylethynylbenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04171373
Source datasetuspto-grants-1979_10
ORD IDord-cfa409b4edc74e79b2e803c699203362
Source noteuspto-grants-1979_10