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Ethanone, 2-chloro-1,2-diphenyl- → 2-(3,4-Methylenedioxyphenyl)-4,5-diphenylthiazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanone, 2-chloro-1,2-diphenyl- | HCID 95343 | — |
| 反応物 | 2H-1,3-benzodioxole-5-carbothioamide | HCID 2776126 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-(3,4-Methylenedioxyphenyl)-4,5-diphenylthiazole | HCID 20344983 | 67.1% |
反応手順
Thiopiperonylamide (18.1 g, 0.10 mole) and desyl chloride (23.1 g, 0.10 mole) are heated under reflux in 95% ethanol (100 ml) for two hours. An oil precipitates which solidifies when the reaction mixture is cooled. The solid is collected and recrystallized from ethanolethyl acetate to give 24.0 g (67% yield ) of 2-(3,4-methylenedioxyphenyl)-4,5-diphenylthiazole, m.p. 121°-124° C. Thiopiperonylamide is also prepared from the corresponding nitrile by the method of Fairfull et al., J. Chem. Soc. 1952, 742.
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-52f6e35e790d48d48e59f5d026142358 |
| 出典メモ | uspto-grants-1980_04 |