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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656593Generated: October 31, 2026

N-Acetyl-4-piperidone → 1-(4-Hydroxypiperidin-1-yl)ethan-1-one

https://huagongshe.com/reaction/1656593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Acetyl-4-piperidoneHCID 122563—
ReactantSodium borohydrideHCID 4311764—
SolventIsopropanolHCID 3776—
Product1-(4-Hydroxypiperidin-1-yl)ethan-1-oneHCID 10749291100%

Reaction Steps

To a cooled (0° C.) mixture of NaBH4 (2.15 g, 0.057 mol) and isopropanol (70 mL) was added N-acetyl-4-piperidone (8.00 g, 0.057 mol). The mixture was allowed to warm to room temperature and stirred for 16 hours. CO2 was bubbled into the reaction mixture, EtOAc (120 mL) was added, and the precipitate was removed by filtration. The filtrate was concentrated to give 8.0 g (100%) of N-acetyl-4-hydroxypiperidine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254689
Source datasetuspto-grants-1993_10
ORD IDord-270cea07e37042d5a8c0128d7e1badc1
Source noteuspto-grants-1993_10