HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267421Generated: October 26, 2026
Sodium borohydride → 5-(3-Hydroxy4-phenyl-butyl)-pyrrolidin-2-one
https://huagongshe.com/reaction/1267421
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(3-Oxo-4-phenyl-butyl)-pyrrolidin-2-one | HCID 12970083 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(3-Hydroxy4-phenyl-butyl)-pyrrolidin-2-one | HCID 12970084 | 72.2% |
Reaction Steps
To a solution of 5-(3-oxo-4-phenyl-butyl)-pyrrolidin-2-one (5.902 g, 25.52 mmol) in EtOH (30 mL) at 0° C. was added NaBH4 (485 mg, 12.76 mmol) and the reaction mixture was stirred at 0° C. for 2.5 h. The reaction mixture was quenched with saturated aqueous ammonium chloride. Water and CH2Cl2 were added. The aqueous layer was washed with CH2Cl2 (2×) and the combined organic extracts were dried (MgSO4), filtered and concentrated. The residue was purified by medium pressure chromatography with a solvent gradient (1:1 hexanes:EtOAc to EtOAc to 1% MeOH in CH2Cl2) to yield 4.3 g of 5-(3-hydroxy-4-phenyl-butyl)-pyrrolidin-2-one. 1H NMR (CDCl3) δ7.35-7.16 (m, 5H), 6.02 (m, 1H), 3.80 (m, 1H), 3.63 (m, 1H), 2.79 (m, 1H), 2.64 (m, 1H), 2.26 (m, 3H), 1.72-1.22 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06552067B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-a4a0464861374d13874e10d1d488243f |
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| Source note | uspto-grants-2003_04 |
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