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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464238Generated: November 1, 2026

Sodium borohydride → 4-Phenyl-4-piperidinocyclohexanol

https://huagongshe.com/reaction/1464238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-Phenyl-4-piperidinocyclohexanoneHCID 13306756—
SolventMethanolHCID 887—
Product4-Phenyl-4-piperidinocyclohexanolHCID 16217185%

Reaction Steps

The cyclohexanone derivative of Example 3 (1 g; 3.9 mmole) was dissolved in 50 ml of methanol inside a three-necked round bottom flask equipped with a condenser. 0.5 g of sodium borohydride was added portionwise to this solution. After addition, the mixture was stirred at room temperature for 2 hours. The methanol was removed under reduced pressure to give a solid residue. The solid residue was extracted with ethyl acetate. The ethyl acetate extracts were combined and washed once with water and dried over anhydrous sodium sulfate. Ethyl acetate was removed to give a solid material. The solid was recrystallized from hexane/ether (1:1; v/v) to give the desired cyclohexanol derivative as a white crystalline solid (0.89 g; 85% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05304479
Source datasetuspto-grants-1994_04
ORD IDord-588b0926c9a84d7c9f5b6440cebad53f
Source noteuspto-grants-1994_04