Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086649Generated: October 31, 2026

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

https://huagongshe.com/reaction/2086649

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 numberUS06727238B2
Source datasetuspto-grants-2004_04
ORD IDord-d1b356ccc29c4a70b8fb513ed8e56b9d
Source noteuspto-grants-2004_04