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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371097Generated: October 30, 2026

Ethyl chloroformate → Ethyl 4-(4-fluorobenzoyl)-4-phenylpiperidine-1-carboxylate

https://huagongshe.com/reaction/371097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant(4-Fluorophenyl)[4-phenyl-1-(phenylmethyl)-4-piperidinyl]methanoneHCID 15586470—
SolventTolueneHCID 1140—
ProductEthyl 4-(4-fluorobenzoyl)-4-phenylpiperidine-1-carboxylateHCID 13477817—

Reaction Steps

To a stirred mixture of 79 parts of (4-fluorophenyl) [4-phenyl-1-(phenylmethyl)-4-piperidinyl]methanone and 630 parts of methylbenzene were added dropwise 32 parts of ethyl carbonochloridate at room temperature. Upon completion, stirring was continued for 5 hours at reflux temperature. The reaction mixture was evaporated and the (chloromethyl)benzene was distilled in vacuo (pump). The oily residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of 2,2'-oxybispropane and a small amount of petroleumether, yielding 35.5 parts of ethyl 4-(4-fluorobenzoyl)-4-phenyl-1-piperidinecarboxylate; mp. 91.7° C. (intermediate 15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04529727
Source datasetuspto-grants-1985_07
ORD IDord-853a05d05d4f49ceb2897af5781b8e0a
Source noteuspto-grants-1985_07