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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant2-(1,2,3-Thiadiazol-4-yl)phenolHCID 2767447—
SolventTolueneHCID 1140—
Product2-(1,2,3-Thiadiazol-4-yl)phenyl isocyanatosulfonateHCID 2039879388.5%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04475944
Source datasetuspto-grants-1984_10
ORD IDord-37c53eb1db0441adbeadea676237c8ec
Source noteuspto-grants-1984_10