HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327700Generated: October 30, 2026
Chlorosulfamic acid → HCID 54170068, compound
https://huagongshe.com/reaction/327700
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosulfamic acid | HCID 24499 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178519020 | HCID 178519020 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54170068 | HCID 54170068 | — |
Reaction Steps
A slurry of 3-hydroxy-4-phenyl-1,2,5-thiadiazole (15.0 g, 0.084 mole) in acetonitrile (100 ml) was treated by the simultaneous dropwise addition of a sulfamoyl chloride solution in acetonitrile (0.20 mole, 66 ml of 3M) and a diisopropylethylamine solution (0.22 mole in enough 1:1 acetonitrile/methylene chloride to make 66 ml). High Pressure Liquid Chromatography analysis indicated a maximum of 85% conversion of starting material to product. The reaction was worked up by concentration of the reaction mixture and partitioning the residue between ethyl ether and water. Concentration of the ether fraction gave a white paste from which desired product was separated by dissolving in a small amount of acetonitrile. The product was crystallized from the acetonitrile to give 2.8 g (13%) of the title compound as a white powder, mp 128°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05273993 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-7862eb4f24d445e19ac37606135d911e |
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| Source note | uspto-grants-1993_12 |
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