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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65264Generated: October 26, 2026

Potassium Hydroxide → alpha-Cyclohexylthiomethyl-beta-(p-methoxyphenyl)-gamma-butyrolactone

https://huagongshe.com/reaction/65264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantCyclohexanethiolHCID 15290—
Reactantalpha-Methanesulfonyloxymethyl-beta-(p-methoxyphenyl)-gamma-butyrolactoneHCID 20234197—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Productalpha-Cyclohexylthiomethyl-beta-(p-methoxyphenyl)-gamma-butyrolactoneHCID 1351897822%

Reaction Steps

To a solution of 480 mg of potassium hydroxide in 40 ml of ethanol were added 2.0 g of α-methanesulfonyloxymethyl-β-(p-methoxyphenyl)-γ-butyrolactone and 1.6 ml of cyclohexylmercaptan and the resulting mixture was kept at room temperature for 4 hours. After completion of the reaction, the reaction mixture was diluted with 200 ml of ethyl ether, washed with water and saturated saline, dried over magnesium sulfate and the solvent was distilled off. The crude product thus obtained was purified by a silica gel column chromatography to give 600 mg (yield 22%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04613613
Source datasetuspto-grants-1986_09
ORD IDord-ba41b964acd849fab487151f8f23f48f
Source noteuspto-grants-1986_09