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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-(3,5-Difluorophenyl)-3,3-dimethylpiperidine-2,4-dione | HCID 66973521 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | cis-6-(3,5-Difluorophenyl)-4-hydroxy-3,3-dimethylpiperidin-2-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629338B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-70acd1bb63d44a129fbbf08fea7df658 |
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| Source note | uspto-grants-2009_12 |
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