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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487166Generated: October 28, 2026

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

https://huagongshe.com/reaction/487166

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 mi of ethanol and 30 ml of water was dissolved 2.93 g of 1-acetyl-4-(4-dimethyiaminobenzoylmethyl)piperidine prepared in Example 39, and at room temperature, 1 9 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 numberUS05294625
Source datasetuspto-grants-1994_03
ORD IDord-cf3b75c033754b758c24c321fc6c8204
Source noteuspto-grants-1994_03