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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089678Generated: November 1, 2026

4-Aminobenzonitrile → 4-{[Cyano(2-fluoro-3-hydroxy-5-methoxyphenyl)methyl]amino}benzonitrile

https://huagongshe.com/reaction/2089678

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobenzonitrileHCID 13396—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Fluoro-3-hydroxy-5-methoxybenzaldehydeHCID 59495309—
CatalystGuanidine HydrochlorideHCID 5742—
SolventMethanolHCID 887—
Product4-{[Cyano(2-fluoro-3-hydroxy-5-methoxyphenyl)methyl]amino}benzonitrileHCID 6746995593.9%

Reaction Conditions

Temperature40 °C

Reaction Steps

Under nitrogen atmosphere, a solution of 2-fluoro-3-hydroxy-5-methoxybenzaldehyde (17.01 g, 100 mmol), 4-aminobenzonitrile (11.81 g, 100 mmol), and guanidine hydrochloride (287 mg, 3 mmol) in methanol (85 mL) was stirred at 40° C. for 1.5 hours. Trimethylsilylcyanide (18.1 mL, 130 mmol) was then added dropwise thereto, and the resulting mixture was stirred at 40° C. for 22 hours. After cooling the mixture, under cooling at 15° C., 3% aqueous sodium hydrogen carbonate solution (87.65 g) was added dropwise thereto, and the resulting mixture was stirred for 1 hour under cooling at 10° C. The precipitated solid was filtered and dried to obtain the captioned compound (27.91 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436009B2
Source datasetuspto-grants-2013_05
ORD IDord-1b2f7d66405c4f43acc7030397091728
Source noteuspto-grants-2013_05