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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756676Generated: October 28, 2026

Ethanol → 1-Acetyl-4-[2-hydroxy-2-(4-dimethylaminophenyl)ethyl]piperidine

https://huagongshe.com/reaction/1756676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
Reactant1-Acetyl-4-(4-dimethylaminobenzoylmethyl)piperidineHCID 19390847—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-Acetyl-4-[2-hydroxy-2-(4-dimethylaminophenyl)ethyl]piperidineHCID 19390848—

Reaction Steps

In a solvent mixture of 60 ml of ethanol and 30 ml of water was dissolved 2.93 g of 1-acetyl-4-(4-dimethylaminobenzoylmethyl)piperidine prepared in Example 39, and at room temperature, 1 g of sodium borohydride was gradually added. The reaction mixture was diluted with dichloromethane and water for distiribution and the dichloromethane layer was dried over anhydrous magnesium sulfate. The solvent was then distilled off and the oily residue was purified by silica gel column chromatography (eluent: ethyl acetate) to give a pale yellow solid melting at 119°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05441967
Source datasetuspto-grants-1995_08
ORD IDord-3469a6ad8bae4a7e8c528a5918b22ce5
Source noteuspto-grants-1995_08