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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106050Generated: October 30, 2026

Benzoyl chloride → HCID 12804767, compound

https://huagongshe.com/reaction/1106050

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 numberUS04311703
Source datasetuspto-grants-1982_01
ORD IDord-e0234696d14c4b50bea6842161eeeb5f
Source noteuspto-grants-1982_01