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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1632439생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1632439

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참여 물질

역할이름HCID투입량
반응물FenadiazoleHCID 13883—
반응물Chlorosulfonyl isocyanateHCID 70918—
용매TolueneHCID 1140—
생성물2-(1,3,4-Oxadiazol-2-yl)phenyl isocyanatosulfonateHCID 1337437559.9%

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온도25 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04475944
출처 데이터셋uspto-grants-1984_10
ORD IDord-d3153606a076463d8f4a41691a379d86
출처 메모uspto-grants-1984_10