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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645871Generated: October 30, 2026

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

https://huagongshe.com/reaction/1645871

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 distribution 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 numberUS05177087
Source datasetuspto-grants-1993_01
ORD IDord-41559a2359ca4016b3421e0fc5928e0d
Source noteuspto-grants-1993_01