関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Fenadiazole | HCID 13883 | — |
| 反応物 | Chlorosulfonyl isocyanate | HCID 70918 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 2-(1,3,4-Oxadiazol-2-yl)phenyl isocyanatosulfonate | HCID 13374375 | 59.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04475944 |
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| 出典データセット | uspto-grants-1984_10 |
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| ORD ID | ord-d3153606a076463d8f4a41691a379d86 |
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| 出典メモ | uspto-grants-1984_10 |
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