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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242618Generated: October 31, 2026

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

https://huagongshe.com/reaction/242618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 23136891HCID 23136891—
Solvent1,2-DichloroethaneHCID 11—
Product4-(2-Chlorophenyl)-4-methylpiperidineHCID 2313698273.4%

Reaction Steps

A solution of 1-benzyl-4-(2-chloro-phenyl)-4-methyl-piperidine (0.59 g, 1.95 mmol) in 1,2-dichloroethane (10 mL) was treated with 1-chloroethyl chloroformate (0.28 mL, 2.6 mmol). This mixture was stirred for 12 hr at reflux, then evaporated in vacuo. The residue was redissolved in methanol (10 mL) and heated to reflux for 1 hr, then evaporated in vacuo. The resulting brown solid (the hydrochloric salt) was washed with ethyl acetate, then freebased with ethyl acetate/sodium hydroxide to yield 0.30 g (72%) of the title compound, ESI-MS m/z: 246 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653096B2
Source datasetuspto-grants-2014_02
ORD IDord-a073c4344ab843f69cdfb4ed56986d72
Source noteuspto-grants-2014_02