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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243752Generated: October 30, 2026

Sodium Hydroxide → 2-(3-Bromo-4-formyl-phenoxy)-4-trifluoromethyl-benzonitrile

https://huagongshe.com/reaction/1243752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-Fluoro-4-(trifluoromethyl)benzonitrileHCID 518973—
ReactantPotassium FluorideHCID 522689—
Reactant2-Bromo-4-hydroxybenzaldehydeHCID 11084866—
SolventDimethylformamideHCID 6228—
Product2-(3-Bromo-4-formyl-phenoxy)-4-trifluoromethyl-benzonitrileHCID 2193034196%

Reaction Steps

2-Fluoro-4-trifluoromethyl-benzonitrile (3.1 g, 20 mmol), 2-bromo-4-hydroxybenzaldehyde (4 g, 20 mmol) and potassium fluoride-(3.47 g, 60 mmol) were heated with stirring in dry DMF (20 mL) at 120° C. for 4 h, 80° C. for 16 h, 120° C. for 4 h, 130° C. for 1 h, and then at 140° C. for 16 h. The reaction mixture was cooled, poured onto 1N sodium hydroxide, extracted with ethyl acetate, and then dried over MgSO4. After filtration, the solvent was removed in vacuo to yield 2-(3-bromo-4-formyl-phenoxy)-4-trifluoromethyl-benzonitrile (6.38 g, 96%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119122B2
Source datasetuspto-grants-2006_10
ORD IDord-be2dd77a220c4b6195246bc332f520ef
Source noteuspto-grants-2006_10