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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164358Generated: November 2, 2026

Ethanol → Ethyl 4-(2-fluorophenyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/1164358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 20511804HCID 20511804—
ProductEthyl 4-(2-fluorophenyl)piperidine-4-carboxylateHCID 2051180668.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 35.8 parts of 4-(2-fluorophenyl)-1-(4-methylphenylsulfonyl)-4-piperidinecarbonitrile and 50 parts of a sulfuric acid solution 75% is stirred for 4 hours at about 150° C. 192 Parts of ethanol are added dropwise. Upon completion, stirring is continued for 5 hours at reflux temperature. The reaction mixture is cooled and poured onto crushed ice. The whole is alkalized with ammonium hydroxide and the product is extracted with dichloromethane. The extract is dried, filtered and evaporated, yielding 17.2 parts (68.4%) of ethyl 4-(2-fluorophenyl)-4-piperidinecarboxylate as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04369184
Source datasetuspto-grants-1983_01
ORD IDord-31ab281da44e465ab89ea166468b19f4
Source noteuspto-grants-1983_01