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Thionyl Chloride → N-benzylidene-4-trifluoromethylbenzenecarbohydrazonoyl chloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | N'-benzylidene-4-trifluoromethylbenzohydrazide | HCID 6736306 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | N-benzylidene-4-trifluoromethylbenzenecarbohydrazonoyl chloride | HCID 86593884 | 59% |
反応手順
A mixture of N′-benzylidene-4-trifluoromethylbenzohydrazide (2.92 g), thionyl chloride (1.09 ml) and toluene (50 ml) was heated under reflux for 1 hr. After cooling, the reaction mixture was concentrated, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=8:1, volume ratio) and recrystallized from hexane to give N-benzylidene-4-trifluoromethylbenzenecarbohydrazonoyl chloride (1.85 g, yield 59%) as pale-yellow plate crystals. melting point: 95–96° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07223791B2 |
| 出典データセット | uspto-grants-2007_05 |
| ORD ID | ord-6a103e3960444c18877c3231eeb865c1 |
| 出典メモ | uspto-grants-2007_05 |