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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52322Generated: October 25, 2026

4-Fluorobenzonitrile → HCID 178504798, compound

https://huagongshe.com/reaction/52322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzonitrileHCID 14517—
Reactant4-(Methylsulfonyl)anilineHCID 79617—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
ProductHCID 178504798HCID 178504798—

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-fluorobenzonitrile (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-fluoro-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-7879e79a639840ceb07086bde3c09b3a
Source noteuspto-grants-1997_04