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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597510Generated: October 25, 2026

Water → 4-Sulfamoylanilino-alpha-[4-(2-furyl)phenyl]acetnitrile

https://huagongshe.com/reaction/1597510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant4-sulfamoyl-N-[4-(2-furyl)benzylidene]anilineHCID 22316731—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
Product4-Sulfamoylanilino-alpha-[4-(2-furyl)phenyl]acetnitrileHCID 2231694572.1%

Reaction Steps

To a suspension of 4-sulfamoyl-N-[4-(2-furyl)benzylidene]aniline (0.37 g, 1.13 mmol) in anhydrous THF (5 mL) at 0° C. was added trimethylsilyl cyanide (0.135 g, 1.36 mmol),zinc chloride (1.36 mL, 1.0 M solution in ether, 1.36 mmol). The temperature of the reaction mixture was then allowed to return to room temperature, and the mixture was stirred overnight. The reaction mixture was poured into water and the whole was extracted with ethyl acetate (20 mL×2). The organic layer was washed with brine, dried over Na2SO4, and concentrated to give the subtitle compound (0.288 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294558B1
Source datasetuspto-grants-2001_09
ORD IDord-90875347bfed4eeb8322a61ca22aaf3e
Source noteuspto-grants-2001_09