Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733321Generated: November 2, 2026

Benzoyl chloride → HCID 12804759, compound

https://huagongshe.com/reaction/1733321

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 numberUS04241071
Source datasetuspto-grants-1980_12
ORD IDord-ba16d3c0cad2450fa4a5bbcb41b641a0
Source noteuspto-grants-1980_12