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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238288Generated: October 30, 2026

1-Chloroethyl chloroformate → 4-(2-Chlorophenyl)-4-methylpiperidine

https://huagongshe.com/reaction/238288

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 15469930HCID 15469930—
ReactantHCID 18675725HCID 18675725—
ReactantHCID 23136891HCID 23136891—
SolventMethanolHCID 887—
Product4-(2-Chlorophenyl)-4-methylpiperidineHCID 23136982—

Reaction Steps

The mixture of 1-benzyl-4-(2-chloro-phenyl)-4-methylpiperidine and 1-benzyl-4-(4-chloro-phenyl)-4-methyl-piperidine (1.6 g) was dissolved in methanol (30 mL) and 1-chloroethylchloroformate (0.9 mL) was added. The mixture was heated at reflux for 10 minutes and allowed to cool. The solvent was removed by evaporation under vacuum and the residue precipitated from ethyl acetate with ether to give a 4:1 mixture of the title compound and 4-(4-chloro-phenyl)-4-methyl-piperidine which was used directly without further purification. LCMS m/z 210.2 [M+H]+. R.T.=2.64 min (Analytical Method 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642621B2
Source datasetuspto-grants-2014_02
ORD IDord-4efed432bd794affafebc2c42892db68
Source noteuspto-grants-2014_02