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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883679Generated: November 1, 2026

Water → 4-[n-(4-Hydroxybenzyl)-n-(4-methoxyphenyl)amino]benzonitrile

https://huagongshe.com/reaction/1883679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant4-((4-Methoxyphenyl)amino)benzonitrileHCID 11333570—
Reactant4-(Tert-butyldimethylsilyloxy)benzyl chlorideHCID 11368885—
SolventDimethylformamideHCID 6228—
Product4-[n-(4-Hydroxybenzyl)-n-(4-methoxyphenyl)amino]benzonitrileHCID 23508515—

Reaction Steps

224 mg of 4-[N(4-methoxyphenyl)amino]benzonitrile was dissolved in 1.2 ml of N,N-dimethylformamide, and 48 mg of sodium borohydride was added thereto under cooling with ice, followed by stirring at room temperature for 30 minutes. The previously prepared 4-(t-butyldimethylsilyloxy)benzyl chloride was dissolved in 1.2 ml of N,N- dimethylformamide and added to the reaction mixture under cooling with ice, followed by stirring at room temperature for 2 days. After water was added to the reaction mixture, the product was extracted with ethyl acetate. After the extract was washed with water and dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was dissolved in 1.2 ml of tetrahydrofuran, and 1.2 ml of a 1 M tetrahydrofuran solution of tetrabutylammonium fluoride was added thereto, followed by stirring at room temperature for 15 minutes. After a saturated aqueous solution of sodium hydrogen carbonate was added to the reaction mixture, the product was extracted with ethyl acetate. After the extract was washed with water and dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (using ethyl acetate as the eluent) to obtain 229 mg of 4-[N-(4-hydroxybenzyl)-N-(4-methoxyphenyl)amino]benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762205B1
Source datasetuspto-grants-2004_07
ORD IDord-458b36073fc7474abd523ee386cf498d
Source noteuspto-grants-2004_07