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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396761Generated: October 25, 2026

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

https://huagongshe.com/reaction/396761

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 numberUS06608095B2
Source datasetuspto-grants-2003_08
ORD IDord-5e2100a86390408d9923e62bc38dceac
Source noteuspto-grants-2003_08