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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088349Generated: October 31, 2026

Dichloromethane → Ethyl 3-(benzyloxy)-4-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/1088349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 15096753HCID 15096753—
SolventTriethylamineHCID 8471—
ProductEthyl 3-(benzyloxy)-4-oxopiperidine-1-carboxylateHCID 301971186.5%

Reaction Steps

To a stirred mixture of 10 parts of 3-(phenylmethoxy)-1-(phenylmethyl)-4-piperidinone and 65 parts of dichloromethane were added dropwise 5 parts of ethyl carbonochloridate at room temperature. After stirring for 6.30 hours at reflux, there were added 5 parts of N,N-diethylethanamine. Upon completion, stirring at reflux was continued for 24 hours. The reaction mixture was washed successively with water, a diluted hydrochloric acid solution and again with water, dried, filtered and evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 8.1 parts (86.5%) of ethyl 4-oxo-3-(phenylmethoxy)-1-piperidinecarboxylate as an oily residue (intermediate 47).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04962115
Source datasetuspto-grants-1990_10
ORD IDord-8c70e145116f4722960992f6da71c1e7
Source noteuspto-grants-1990_10