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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635709Generated: October 30, 2026

Water → HCID 18676556, compound

https://huagongshe.com/reaction/1635709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-Acetylsulfanilyl chlorideHCID 8481—
ReactantCalcium CarbonateHCID 10112—
ReactantIci 222155HCID 195716—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18676556HCID 186765567.2%

Reaction Steps

2.9 g (12.4 mmol) of N-acetylsulphanilyl chloride are added portionwise to a mixture, maintained under a nitrogen atmosphere, of 2.0 g (8.19 mmol) of 3,5-dimethyl-4-[(nitromethyl)sulphonyl]aniline and 1.6 g (16.0 mmol) of calcium carbonate in 40 ml of anhydrous tetrahydrofuran. The reaction medium is stirred for 6 h at room temperature and is then refluxed for 2 h, after which it is poured into 200 ml of water. The mixture is extracted 3 times with methylene chloride. The combined organic extracts are washed with water, dried over sodium sulphate and concentrated to dryness under reduced pressure. The oily residue obtained is crystallized by trituration from a mixture of hexane and ethyl acetate. These crystals are washed with a mixture of methylene chloride and methanol at room temperature and then with a mixture of hexane and ethyl acetate at reflux, and finally with ethanol at room temperature, to give 0.26 g (7.2%) of N-[4-[3,5-dimethyl-4-[(nitromethyl)sulphonyl]phenylsulphamoyl]phenyl]acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509499B1
Source datasetuspto-grants-2003_01
ORD IDord-8d9e34177ef6495f952a219818044a5e
Source noteuspto-grants-2003_01