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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166348Generated: October 31, 2026

Benzonitrile, 4-(trifluoromethyl)- → HCID 178504795, compound

https://huagongshe.com/reaction/1166348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrile, 4-(trifluoromethyl)-HCID 67995—
Reactant4-(Methylsulfonyl)anilineHCID 79617—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
ProductHCID 178504795HCID 178504795—

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 4-trifluoromethylbenzonitrile (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 4-(trifluoromethyl)-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide is used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613789B2
Source datasetuspto-grants-2003_09
ORD IDord-1968365d91984f69a327468326313546
Source noteuspto-grants-2003_09