HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981261Generated: October 25, 2026
Fenadiazole → 2-(1,3,4-Oxadiazol-2-yl)phenyl isocyanatosulfonate
https://huagongshe.com/reaction/1981261
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Fenadiazole | HCID 13883 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(1,3,4-Oxadiazol-2-yl)phenyl isocyanatosulfonate | HCID 13374375 | 59.9% |
Reaction Steps
By the procedure of Example 1, 7.1 g of chlorosulfonyl isocyanate was added to a suspension containing 8.1 g of 2-(1,3,4-oxadiazol-2-yl)phenol [prepared by the procedure of J. Maillard et al., Bull. Soc. Chim. France, 3, 529 (1961)] 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 about 0.5 hour. The resulting suspension containing a viscous oil was cooled to 25° C., filtered, and the filtrate was concentrated in vacuo to yield 8 g of the title compound as a viscous, crude oil. The IR spectrum showed an isocyanate absorption at 2220 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04514214 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-f9f04c7e7c024970b87aefd16a9881a2 |
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| Source note | uspto-grants-1985_04 |
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