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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373122Generated: November 1, 2026

Water → HCID 18005695, compound

https://huagongshe.com/reaction/1373122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Chloro-N,N-dimethylethylamineHCID 7901—
ReactantN-(3-nitrophenyl)methanesulfonamideHCID 843283—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 18005695HCID 18005695—

Reaction Steps

5 g (23.1 mmol) of 3-methylsulphonylamino-nitrobenzene are dissolved in 50 ml of DMSO and combined with 6.5 g (58 mmol) of potassium tert. butoxide while cooling with ice. The solution thus obtained is added dropwise to a solution of 5 g (34.7 mmol) of 2-chloro-N,N-dimethyl-ethylamine in 30 ml of DMSO. The mixture is stirred for 2 hours at ambient temperature and then heated for 6 hours to 100° C. After cooling to ambient temperature 400 ml of water are added. The mixture is extracted with ethyl acetate. Water and 1 N hydrochloric acid are added to the combined organic phases until an acid reaction is obtained. The aqueous phase is washed with ethyl acetate. Then the aqueous phase is made alkaline with sodium carbonate and the product is extracted with ethyl acetate. Drying the combined organic phases over magnesium sulphate and eliminating the solvents in vacuo yields the product as a red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160901B2
Source datasetuspto-grants-2007_01
ORD IDord-fb9e7a6b02d54dbc932918623ff594f6
Source noteuspto-grants-2007_01