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HRID 1632439作成日:2026年10月26日

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

https://huagongshe.com/reaction/1632439

反応式

関与物質

役割名称HCID仕込み量
反応物FenadiazoleHCID 13883—
反応物Chlorosulfonyl isocyanateHCID 70918—
溶媒TolueneHCID 1140—
生成物2-(1,3,4-Oxadiazol-2-yl)phenyl isocyanatosulfonateHCID 1337437559.9%

反応条件

温度25 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04475944
出典データセットuspto-grants-1984_10
ORD IDord-d3153606a076463d8f4a41691a379d86
出典メモuspto-grants-1984_10