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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050443Generated: November 1, 2026

4-Fluorobenzoyl chloride → HCID 178525712, compound

https://huagongshe.com/reaction/2050443

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantHCID 178521563HCID 178521563—
SolventPyridineHCID 1049—
ProductHCID 178525712HCID 178525712—

Reaction Steps

A solution of 1.7 g of 4-fluorobenzoyl chloride in 5 ml of pyridine is treated with 2.8 g of trans-4-[trans-4-[2-(1,3-dioxolan-2-yl)ethyl]cyclohexyl]cyclohexanol (prepared according to Example 1) and stirred at room temperature for 12 hours. Thereafter, the reaction mixture is poured on to ice-water and extracted three times with diethyl ether. The organic phases are washed in succession with saturated sodium hydrogen carbonate solution, with 10 percent hydrochloric acid, with saturated sodium hydrogen carbonate solution and with water, then dried over magnesium sulfate, filtered and concentrated. Chromatographic purification of the resulting crude product on silica gel with ethyl acetate/petroleum ether (vol. 3:97) gives 4-fluorobenzoic acid trans-4-[trans-4-[2-(1,3-dioxolan-2-yl)ethyl]cyclohexyl]cyclohexyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013477
Source datasetuspto-grants-1991_05
ORD IDord-36e59ce4246c4e6b862eaa901af70843
Source noteuspto-grants-1991_05