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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593614Generated: November 1, 2026

Potassium Hydroxide → Ethyl 4-[(4-fluorophenyl)thio]-3-oxocyclohexanecarboxylate

https://huagongshe.com/reaction/1593614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4-FluorothiophenolHCID 67789—
ReactantEthyl 4-bromo-3-oxocyclohexanecarboxylateHCID 12917736—
SolventEthanolHCID 702—
ProductEthyl 4-[(4-fluorophenyl)thio]-3-oxocyclohexanecarboxylateHCID 6923223551%

Reaction Steps

To a solution of ethyl 4-bromo-3-oxocyclohexanecarboxylate (5.2 g, 20.9 mmol) in EtOH (120 mL) at 80° C. was added a solution of 4-fluorobenzenethiol (2.22 mL, 20.9 mmol) and KOH (1.29 g, 22.9 mmol) in EtOH (50 mL). The suspension was stirred for 30 min then filtered. The filtrate was concentrated in vacuo then diluted with water and extracted with diethyl ether. The organic layer was washed with water then brine, then was dried over MgSO4 and concentrated in vacuo. Purification by chromatography on silica gel (15% EtOAc in hexane) afforded the title compound (3.08 g, 51%) as a white solid: mp 96-97° C.; MS (+) 297 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297704B2
Source datasetuspto-grants-2007_11
ORD IDord-cb0ca5ebfb5a44d4acdc83b3ed4b97d6
Source noteuspto-grants-2007_11