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4-Chloro-1-(2-thienyl)butan-1-one → 2-[4-Chloro-1-(thiophen-2-yl)-butylidene]-hydrazinecarbothioamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Chloro-1-(2-thienyl)butan-1-one | HCID 123511 | — |
| 反応物 | Thiosemicarbazide | HCID 2723789 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-[4-Chloro-1-(thiophen-2-yl)-butylidene]-hydrazinecarbothioamide | HCID 54569609 | 57% |
反応手順
Thiosemicarbazide (9.11 g, 0.1 mol) was added under nitrogen to a solution 4-chloro-2'-butyrothienone (16.2 mL, 0.1 mol) in 350 mL of methanol plus 27 mL 1N HCl plus 25 mL of water. After stirring at room temperature for approximately 2 hours, all of the solid had dissolved. The reaction was then stirred at room temperature for 24 hours (overnight). By TLC starting material remained. An additional 27 mL of 1N HCl was added and the reaction stirred at room temperature for 6 hours. The solid formed was removed by filtration and dried under high vacuum to give 14.87 g (57%) of the title compound as a brown solid, mp 120-122° 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-08f667f3cc214dae90b9d0e45627e7c1 |
| 出典メモ | uspto-grants-1999_12 |