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4-Chlorobutyrophenone → 2-(4-Chloro-1-phenyl-butylidene)-N-phenyl-hydrazinecarbothioamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Chlorobutyrophenone | HCID 253533 | — |
| 反応物 | Hydrazinecarbothioamide, N-phenyl- | HCID 730679 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-(4-Chloro-1-phenyl-butylidene)-N-phenyl-hydrazinecarbothioamide | HCID 53747260 | 62.6% |
反応手順
A mixture of 4-chlorobutyrophenone (6.7 mL, 42 mmol) and 4-phenyl-3-thiosemicarbazide (7.0 g, 42 mmol) in 500 mL of ethanol was warmed under a nitrogen atmosphere to dissolve all the solids and then the reaction stirred at room temperature for four days. The solid formed was collected by filtration and dried under reduced pressure to give 8.73 g of a white solid. Recrystallization of the solid from ethanol gave 7.99 g (57%) of the title compound as a white solid, mp 107-109° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06008362 |
| 出典データセット | uspto-grants-1999_12 |
| ORD ID | ord-a4ace6d1b5ed443c8dd624f2fd2543b9 |
| 出典メモ | uspto-grants-1999_12 |