HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164417Generated: November 1, 2026
Chlorosulfonyl isocyanate → HCID 20405594, compound
https://huagongshe.com/reaction/2164417
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | HCID 13145814 | HCID 13145814 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20405594 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04504490 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-87f567a010b64259ae0573954fad5d5d |
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| Source note | uspto-grants-1985_03 |
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