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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867396Generated: October 25, 2026

1-Benzyl-3-methyl-4-piperidone → 1-Benzyl-3-methylpiperidin-4-ol

https://huagongshe.com/reaction/1867396

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-3-methyl-4-piperidoneHCID 560965—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product1-Benzyl-3-methylpiperidin-4-olHCID 13611492102.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Benzyl-3- methyl-piperidin-4-one (2.0 g, 10 mmol) was dissolved in MeOH (10 ml), cooled to 0° C. and sodium borohydride (0.2 g, 5 mmol) was added portionwise. The reaction was allowed to reach room temperature and stirred overnight after which time the solvent was removed under vacuum, the residue redissolved in CH2Cl2, washed with water, dried (Na2SO4) and concentrated to afford the title compound (2.1 g, quant), a 3:1 mixture of diasteriomers (trans:cis) as gum. MS: 206.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632829B2
Source datasetuspto-grants-2009_12
ORD IDord-11463f45e6604c3e94b264e4044cc1bd
Source noteuspto-grants-2009_12