HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632441Generated: October 25, 2026
Chlorosulfonyl isocyanate → 2-(1,2,3-Thiadiazol-4-yl)phenyl isocyanatosulfonate
https://huagongshe.com/reaction/1632441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 2-(1,2,3-Thiadiazol-4-yl)phenol | HCID 2767447 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(1,2,3-Thiadiazol-4-yl)phenyl isocyanatosulfonate | HCID 20398793 | 88.5% |
Reaction Steps
By the procedure of Example 1, 7.9 g of chlorosulfonyl isocyanate was reacted with 10 g of 2-(1,2,3-thiadiazol-4-yl)phenol [prepared by the procedure of U.S. Pat. No. 3,940,407] in 125 ml of dry toluene. The reaction mixture was stirred at 25° C. for 1 hour, then heated at 100° to 110° C. for 1 hour. The resulting solution was cooled to 25° C., filtered, and the filtrate was concentrated in vacuo to yield 14 g of the title compound as a crude oil. The IR showed an isocyanate absorption at 2220 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04475944 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-37c53eb1db0441adbeadea676237c8ec |
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| Source note | uspto-grants-1984_10 |
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