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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503921Generated: October 31, 2026

Sodium borohydride → (S)-3-(4-bromo-2-methoxy-phenyl)-4-hydroxy-butyronitrile

https://huagongshe.com/reaction/503921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(S)-3-(4-bromo-2-methoxy-phenyl)-4-((S)-4-isopropyl-2-oxo-oxazolidin-3-yl)-4-oxo-butyronitrileHCID 66877211—
ReactantKHSO4 Na2SO4HCID 86586342—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(S)-3-(4-bromo-2-methoxy-phenyl)-4-hydroxy-butyronitrileHCID 6687654092%

Reaction Steps

A solution of sodium borohydride (389 mg) in water (1.82 mL) was added to a solution of (S)-3-(4-bromo-2-methoxy-phenyl)-4-((S)-4-isopropyl-2-oxo-oxazolidin-3-yl)-4-oxo-butyronitrile (749 mg, 1.895 mmol) in THF (6 mL) under nitrogen atmosphere. The mixture was stirred at room temperature for three hours. The reaction mixture was cooled to 0° C. and a solution of 10% KHSO4/Na2SO4 was carefully added. After the gas evolution stopped, the mixture was extracted with EtOAc. The combined organic extracts were washed with brine, dried over Na2SO4, filtered, and evaporated under reduced pressure. The residue was purified via flash chromatography (hexane/EtOAc, 7/3) to give 470 mg (92% yield) of (S)-3-(4-bromo-2-methoxy-phenyl)-4-hydroxy-butyronitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776910B2
Source datasetuspto-grants-2010_08
ORD IDord-f22e4a1567ea4a959e34c5a9adc7a720
Source noteuspto-grants-2010_08