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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFenadiazoleHCID 13883—
ReactantChlorosulfonyl isocyanateHCID 70918—
SolventTolueneHCID 1140—
Product2-(1,3,4-Oxadiazol-2-yl)phenyl isocyanatosulfonateHCID 1337437559.9%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04514214
Source datasetuspto-grants-1985_04
ORD IDord-f9f04c7e7c024970b87aefd16a9881a2
Source noteuspto-grants-1985_04