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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980134Generated: October 31, 2026

Ethyl chloroformate → Ethyl 4-[(4-fluorophenyl)(3-pyridinyl)methylene]-1-piperidinecarboxylate

https://huagongshe.com/reaction/1980134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant3-[(4-Fluorophenyl)(1-methyl-4-piperidinylidene)methyl]pyridineHCID 13520016—
SolventChloroformHCID 6212—
ProductEthyl 4-[(4-fluorophenyl)(3-pyridinyl)methylene]-1-piperidinecarboxylateHCID 2332607975%

Reaction Steps

To a stirred solution of 180 parts of ethyl carbonochloridate in 600 parts of trichloromethane was added dropwise a solution of 110 parts of 3-[(4-fluorophenyl)(1-methyl-4-piperidinylidene)-methyl]pyridine in 600 parts of trichloromethane. Upon completion, the whole was heated till reflux and stirring at reflux was continued for 16 hours. The reaction mixture was evaporated. The residue was stirred in water and the whole was alkalized with a sodium hydroxide solution. The product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated, yielding 100 parts (75%) of ethyl 4-[(4-fluorophenyl)(3-pyridinyl)methylene]-1-piperidinecarboxylate as a residue (intermediate 20).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04485107
Source datasetuspto-grants-1984_11
ORD IDord-2556e0dbbc40440a9a1b83f63199507d
Source noteuspto-grants-1984_11