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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52294Generated: October 26, 2026

4-Chlorobenzonitrile → 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide

https://huagongshe.com/reaction/52294

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzonitrileHCID 12163—
Reactant4-(Methylsulfonyl)anilineHCID 79617—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
Product4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamideHCID 178504796—

Reaction Steps

To a suspension of 4-(methylsulfonyl)aniline (7 g, 41 mmol) in toluene (400 mL), trimethylaluminum (2M solution in toluene, 30.5 mL, 61 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 2.5 hours. A solution of 4-chlorobenzonitrile (11.3 g, 82 mmol) in toluene (200 mL) was added over 10 minutes and the reaction mixture was heated to 80°-85° C. After 16 hours, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the residue was washed with a mixture of methylene chloride/methanol. The combined filtrates were concentrated in vacuo and the resulting yellowish solid was stirred with a mixture of hexane/ether (2/1, 1000 mL). The intermediate was filtered and washed with more of hexane/ether (2/1). The pale yellow solid 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (10.93 g, 86%) was used in the next reaction without further purification: mp (DSC) 191° C. Anal. Calc'd. for C14H13N2SO2Cl: C, 54.46, H, 4.24, N, 9.07. Found: C, 54.42, H, 4.30, N, 9.07.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616601
Source datasetuspto-grants-1997_04
ORD IDord-45e2e30cff9d4228995f8b63eba08d26
Source noteuspto-grants-1997_04