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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474553Generated: October 30, 2026

Sodium Hydroxide → (E)-3-(3-Bromo-4-fluorophenyl)acrylonitrile

https://huagongshe.com/reaction/474553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-Bromo-4-fluorobenzaldehydeHCID 173604—
Reactant(Cyanomethyl)triphenylphosphonium bromideHCID 11811037—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(E)-3-(3-Bromo-4-fluorophenyl)acrylonitrileHCID 61702072125.9%

Reaction Steps

To a mixture of (cyanomethyl)triphenylphosphonium bromide (70.6 g, 185 mmol) and sodium hydroxide (7.39 g, 185 mmol) in DCM (100 mL) and water (300.00 mL) at 0° C. was added 3-bromo-4-fluorobenzaldehyde (25.0 g, 123 mmol). It was allowed to warm to room temperature and stirred for 2 h. The organic layer was separated, and the water layer was extracted with DCM twice. The combined organic phases were dried over Na2SO4 and concentrated to give a crude product, which was washed with diethyl ether. The residue was purified to give the title compound as a white solid (35 g, 88% yield). LCMS: rt=1.50 min, [M+H+]=226

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-99c933f36cb64fdb8139b594bd3d64b7
Source noteuspto-grants-2014_01