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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227755Generated: October 31, 2026

Benzenesulfonyl chloride → N-(4-[2-Methyl-2-aminopropyl]phenyl)benzenesulfonamide

https://huagongshe.com/reaction/2227755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant4-(2-Amino-2-methylpropyl)aniline hydrochloride saltHCID 22147754—
SolventDimethylformamideHCID 6228—
ProductN-(4-[2-Methyl-2-aminopropyl]phenyl)benzenesulfonamideHCID 2214770138%

Reaction Steps

A solution of 4-(2-amino-2-methylpropyl)aniline hydrochloride salt (1.0 g, 4.98 mmol) in anhydrous DMF (30 mL) was treated with benzenesulfonyl chloride (880 mg, 4.98 mmol). The solution was stirred at ambient temperature for 16 h. The solvent was removed under reduced pressure and the residue was washed twice with hexane. The insoluble material was dissolved in water and extracted twice with ethyl ether to remove any remaining neutral impurities. The aqueous layer was separated and basified with excess 1N sodium hydroxide. Upon standing, a crystalline solid soon precipitated. The solid was collected, and dried under vacuum at 60° C. to provide 570 mg (38%) of the desired product as a white crystalline solid. Mp 180-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413991B1
Source datasetuspto-grants-2002_07
ORD IDord-6222f1a81c7e4599b098dc482418f532
Source noteuspto-grants-2002_07