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2-Propanone, 1-bromo-1-phenyl- → 2-(2-Chlorophenyl)-4-methyl-5-phenylthiazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Propanone, 1-bromo-1-phenyl- | HCID 90870 | — |
| 反応物 | 2-Chlorothiobenzamide | HCID 2734824 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-(2-Chlorophenyl)-4-methyl-5-phenylthiazole | HCID 20344980 | 79.1% |
反応手順
1-Bromo-1-phenyl-2-propanone (10.6 g, 0.050 mole), o-chlorothiobenzamide (8.8 g, 0.051 mole), and ethanol (100 ml) are mixed and, after the initial exothermic reaction has subsided, heated under reflux for two hours. The ethanol is evaporated and the residue is treated with chloroform and aqueous sodium bicarbonate. The chloroform layer is separated and evaporated to leave a yellow oil which solidifies on standing. Recrystallization from acetonitrile yields 11.3 g (79%) of 2-(2-chlorophenyl)-4-methyl-5-phenylthiazole, m.p. 63°-65° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04197306 |
| 出典データセット | uspto-grants-1980_04 |
| ORD ID | ord-6c5df390d09c4601bfba77809ba65231 |
| 出典メモ | uspto-grants-1980_04 |