関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Difluoromethane | HCID 6345 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | HCID 178527949 | HCID 178527949 | — |
| 触媒 | Potassium Iodide | HCID 4875 | — |
| 触媒 | Tributylammonium bromide | HCID 13798051 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 2-Difluoromethylthio-5-pyrid-2-yl-1,3,4-thiadiazole | HCID 19870488 | 75.1% |
反応手順
A suspension of 341.5 g (l.75 mol) of 2-mercapto-5-pyrid-2-yl-1,3,4-thiadiazole in 4000 ml of dioxane is added to a solution of 230.5 g of 85% potassium hydroxide in 800 ml of water. Then 10 g of potassium iodide and 6 g of tributylammonium bromide are added to the reaction mixture and 750 g (~8.6 mol) of gaseous difluoromethane are introduced over 41/2 hours at 22°-37° C. After evaporating off the dioxane, the reaction mixture is diluted with ethyl acetate, the aqueous phase is separated and the organic solution is washed cold with 1N sodium hydroxide and water, dried over sodium sulfate and clarified with activated carbon. They ethyl acetate is removed under vacuum and the residue is crystallised from ethyl acetate/hexane, affording 321.9 g (75.1%) of the title compound with a melting point of 90°-92° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04894380 |
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| 出典データセット | uspto-grants-1990_01 |
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| ORD ID | ord-9ec7e6f0f65c41ab83ae5aecb742d22c |
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| 出典メモ | uspto-grants-1990_01 |
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