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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52325Generated: October 26, 2026

Benzonitrile → HCID 178504794, compound

https://huagongshe.com/reaction/52325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrileHCID 7505—
Reactant4-(Methylsulfonyl)anilineHCID 79617—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
ProductHCID 178504794HCID 178504794—

Reaction Steps

To a suspension of 4-(methylsulfonyl)aniline (10 mmol) in toluene (100 mL), trimethylaluminum (2M solution in toluene, 15 mmol) is added over 15 minutes. The reaction mixture is warmed to room temperature and stirred for 2.5 hours. A solution of benzonitrile (20 mmol) in toluene (50 mL) is added over 10 minutes and the reaction mixture is heated to 80°-85° C. After 20 hours, the reaction mixture is cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the residue is washed with a mixture of methylene chloride/methanol (2/1). The combined filtrates are concentrated in vacuo and the resulting yellowish solid is stirred with a mixture of hexane/ether (2/1, 1000 mL). The intermediate is filtered and washed with more of hexane/ether (2/1). The pale yellow solid N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide is used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616601
Source datasetuspto-grants-1997_04
ORD IDord-f2ccdff770764ae6a8f9beff10fe80b0
Source noteuspto-grants-1997_04