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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866655Generated: November 1, 2026

Sodium borohydride → cis-6-(3,5-Difluorophenyl)-4-hydroxy-3,3-dimethylpiperidin-2-one

https://huagongshe.com/reaction/1866655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant6-(3,5-Difluorophenyl)-3,3-dimethylpiperidine-2,4-dioneHCID 66973521—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Productcis-6-(3,5-Difluorophenyl)-4-hydroxy-3,3-dimethylpiperidin-2-oneHCID 66973592—

Reaction Steps

To a solution of 6-(3,5-difluorophenyl)-3,3-dimethylpiperidine-2,4-dione from Step A (20.18 g, 80 mmol) in THF (600 mL) and CH3OH (25 mL) at 0° C. was added NaBH4 (4.57 g, 121 mmol). After 2.5 h, the reaction mixture was quenched with H2O (200 mL) and concentrated in vacuo. The residue was partitioned between H2O (600 mL), saturated aqueous NaHCO3 (200 mL) and EtOAc (1 L). The organic layer was separated and the aqueous layer was extracted with EtOAc (600 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:CH3OH—100:0 to 88:12, to give the title compound, which contained approximately 20% of the corresponding trans-isomer. MS: m/z=256 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629338B2
Source datasetuspto-grants-2009_12
ORD IDord-70acd1bb63d44a129fbbf08fea7df658
Source noteuspto-grants-2009_12