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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733324Generated: November 3, 2026

Benzoyl chloride → HCID 12804767, compound

https://huagongshe.com/reaction/1733324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 12804754HCID 12804754—
SolventDiethyl EtherHCID 3283—
ProductHCID 12804767HCID 12804767—

Reaction Steps

1.5 g of 1-methyl-4[α-(2-fluoro-4-methylphenyl)-2-tolyl]-4-piperidinol, Example 4, is treated carefully with 7 ml of benzoyl chloride with stirring and cooling. The reaction mixture is stirred for 16 hours at ambient temperature and then diluted with 15 ml of ether. The resulting precipitate is filtered, washed with ether, converted to the free base which is column chromatographed on an alumina column using ether as the eluant. The free base is converted to its hydrogen chloride salt which is recrystallized from a methanol-acetone-ether mixture to give a white powder, mp 218°-219° C. of 4-benzoyloxy-4-[α-(2-fluoro-4-methylphenyl)-2-tolyl]-1-methylpiperidine hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04241071
Source datasetuspto-grants-1980_12
ORD IDord-402ca8d5d32840ffaedbf7e0e75de002
Source noteuspto-grants-1980_12