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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164364Generated: November 5, 2026

Sodium borohydride → HCID 13094167, compound

https://huagongshe.com/reaction/1164364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13094166HCID 13094166—
SolventEthanolHCID 702—
ProductHCID 13094167HCID 1309416735%

Reaction Steps

To a stirred mixture of 4.5 parts of ethyl 1-[4-cyano-4-(2-pyridinyl)-1-cyclohexenyl]-4-phenyl-4-piperidinecarboxylate and 80 parts of ethanol are added portionwise 0.4 parts of sodium borohydride. Upon completion, stirring is continued first overnight at room temperature and further for 30 minutes at reflux. The reaction mixture is cooled and poured onto water. The product is extracted with dichloromethane. The extract is dried, filtered and evaporated. The residue is crystallized from 2-propanol, yielding 2 parts (35%) of ethyl 1-[4-cyano-4-(2-pyridinyl)cyclohexyl]-4-phenyl-4-piperidinecarboxylate; mp. 157.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04369184
Source datasetuspto-grants-1983_01
ORD IDord-9bd39efd566e4ffdb12b28a532a07b97
Source noteuspto-grants-1983_01