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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635705Generated: October 27, 2026

Water → 4-bromo-N-[3,5-dimethyl-4-[(nitromethyl)sulphonyl]phenyl]benzenesulphonamide

https://huagongshe.com/reaction/1635705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
ReactantCalcium CarbonateHCID 10112—
ReactantIci 222155HCID 195716—
SolventTetrahydrofuranHCID 8028—
Product4-bromo-N-[3,5-dimethyl-4-[(nitromethyl)sulphonyl]phenyl]benzenesulphonamideHCID 1867654024.2%

Reaction Steps

2.0 g (20.0 mmol) of calcium carbonate and 3.8 g (14.9 mmol) of 4-bromobenzenesulphonyl chloride are successively added to a mixture of 2.4 g (9.83 mmol) of 3,5-dimethyl-4-[(nitromethyl)sulphonyl]aniline in 45 ml of anhydrous tetrahydrofuran. The reaction medium is stirred for 20 h at room temperature and is then refluxed for 48 h. After cooling, it is poured into 400 ml of water and extracted with methylene chloride. The combined organic extracts are dried over sodium sulphate and concentrated to dryness under reduced pressure. The oily residue obtained is purified by chromatography on a column of silica (eluent: methylene chloride) to give 1.1 g (24%) of 4-bromo-N-[3,5-dimethyl-4-[(nitromethyl)sulphonyl]phenyl]benzenesulphonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509499B1
Source datasetuspto-grants-2003_01
ORD IDord-b40e833edb224f349c1bd9d6ac3cf4fd
Source noteuspto-grants-2003_01