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Triethylamine → 5-(N-Methyl-Trichloromethylthioamino)-3-Trichloromethyl-1,2,4-Thiadiazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Trichloromethanesulfenyl chloride | HCID 11666 | — |
| 反応物 | N-Methyl-3-(trichloromethyl)-1,2,4-thiadiazol-5-amine | HCID 13150493 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 5-(N-Methyl-Trichloromethylthioamino)-3-Trichloromethyl-1,2,4-Thiadiazole | HCID 20288720 | 23% |
反応手順
To a 3-neck flask equpped with condenser, thermometer and stirring bar was added 11.6 g (0.05 mole) 5-methylamino-3-trichloromethyl-1,2,4- thiadiazole, 5.1 g (0.05 mole) triethylamine and 150 milliliters of benzene. After 9.3 g (0.05 mole) trichloromethane-sulfenyl chloride was added, the reaction mixture was heated at reflux for 20 hours and filtered hot. The filtrate was evaporated under vacuum to give a beige solid which was refluxed in 400 milliliters of ligroin and filtered. The ligroin was cooled, filtered and the filtrate evaporated to 20 milliliters and filtered. The resulting solid was recrystallized again from ligroin to obtain 4.4 g (23% yield) of product; mp=106° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04254265 |
| 出典データセット | uspto-grants-1981_03 |
| ORD ID | ord-4904e7b964b44603a8858fcc6ee29db7 |
| 出典メモ | uspto-grants-1981_03 |