Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164417Generated: November 1, 2026

Chlorosulfonyl isocyanate → HCID 20405594, compound

https://huagongshe.com/reaction/2164417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantHCID 13145814HCID 13145814—
SolventTolueneHCID 1140—
ProductHCID 20405594HCID 20405594—

Reaction Steps

30 ml of N-chlorosulfonyl isocyanate are added dropwise, at +10° C., to 108 g of 2-amino-5-(3-trifluoromethylphenylsulfonyloxy)nitrobenzene in 800 ml of toluene. The mixture is stirred for a further two hours while cooling, and 500 ml of petroleum ether are added. The 2-(3-chlorosulfonylureido)-5-(3-trifluoromethylphenylsulfonyloxy)nitrobenzene produced is filtered off with suction, washed with petroleum ether and dried over potassium hydroxide, melting point 137° C., decomposition. 150 g of this sulfochloride are introduced, with stirring and cooling in ice, into 2 liters of 1N HCl. The mixture is stirred for 2 hours while cooling and for 5 hours at room temperature, and next day the precipitate is filtered off with suction, washed with water to neutrality and dried, melting point 152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04504490
Source datasetuspto-grants-1985_03
ORD IDord-87f567a010b64259ae0573954fad5d5d
Source noteuspto-grants-1985_03