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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484722Generated: October 30, 2026

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

https://huagongshe.com/reaction/484722

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 numberUS04533665
Source datasetuspto-grants-1985_08
ORD IDord-bcdb26e60dad40998c99c74b04b7b1ee
Source noteuspto-grants-1985_08