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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648910Generated: October 31, 2026

Benzoyl chloride → HCID 12804759, compound

https://huagongshe.com/reaction/1648910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 12542600HCID 12542600—
SolventDiethyl EtherHCID 3283—
ProductHCID 12804759HCID 12804759—

Reaction Steps

2.0 g of 1-methyl-4-(α-phenyl-2-tolyl)-4-piperidinol, Example 1, is treated with 10 ml of benzoyl chloride with stirring and cooling. The reaction solution is diluted with 20 ml of ether, stirred for two hours and the resulting precipitate collected by suction filtration. The filter cake is washed well with ether and dried in vacuo at 40° C. over sodium hydroxide pellets. The dried filter cake is recrystallized twice from a chloroform-ether mixture to give colorless crystals, mp 197°-198° C. of 4-benzoyloxy-1-methyl-4-(α-phenyl-2-tolyl)piperidine hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04414219
Source datasetuspto-grants-1983_11
ORD IDord-8b2edaa958ac4100abeb33d6280eeadf
Source noteuspto-grants-1983_11