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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503908Generated: November 2, 2026

Lithium borohydride → 2-(4-Bromo-2-methyl-phenyl)-4-hydroxy-butyronitrile

https://huagongshe.com/reaction/503908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
Reactant3-(4-Bromo-2-methyl-phenyl)-3-cyano-propionic acid methyl esterHCID 66877131—
ReactantKHSO4 Na2SO4HCID 86586342—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Bromo-2-methyl-phenyl)-4-hydroxy-butyronitrileHCID 5942833487%

Reaction Conditions

Temperature0 °C

Reaction Steps

Lithium borohydride (4.99 g, 0.2290 mol) was added to a room temperature solution of 3-(4-bromo-2-methyl-phenyl)-3-cyano-propionic acid methyl ester (43.08 g, 0.1527 mol) in THF (500 mL) and the reaction mixture was stirred overnight. The reaction mixture was cooled to 0° C., and a solution of 10% KHSO4/Na2SO4 was slowly added until pH 1-2 was reached. The resulting mixture was extracted with EtOAc, and the combined organic extracts were washed with water and brine, dried over Na2SO4, filtered, and evaporated under reduced pressure. The residue was purified via flash chromatography (hexane/EtOAc, 7/3) to give 27.3 g (87% yield) of 2-(4-bromo-2-methyl-phenyl)-4-hydroxy-butyronitrile as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776910B2
Source datasetuspto-grants-2010_08
ORD IDord-9e7375483a8e47399aedbb2bb604d1d2
Source noteuspto-grants-2010_08