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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1632439Erstellt: 25. Oktober 2026

Fenadiazole → 2-(1,3,4-Oxadiazol-2-yl)phenyl isocyanatosulfonate

https://huagongshe.com/reaction/1632439

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFenadiazoleHCID 13883—
EduktChlorosulfonyl isocyanateHCID 70918—
LösungsmittelTolueneHCID 1140—
Produkt2-(1,3,4-Oxadiazol-2-yl)phenyl isocyanatosulfonateHCID 1337437559,9%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04475944
Quelldatensatzuspto-grants-1984_10
ORD IDord-d3153606a076463d8f4a41691a379d86
Quellennotizuspto-grants-1984_10