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Hydrazine → 6-(4-Bromophenyl)-4,5-dihydropyridazin-3(2H)-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrazine | HCID 9321 | — |
| 反応物 | 3-(4-Bromobenzoyl)propionic acid | HCID 80646 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 6-(4-Bromophenyl)-4,5-dihydropyridazin-3(2H)-one | HCID 689108 | 97.5% |
反応手順
A solution of 4-(4-bromo-phenyl)-4-oxo-butyric acid (Aldrich, 25.0 g, 97.3 mmol) in EtOH (100 mL) was treated with aqueous hydrazine (Aldrich, 55%, 9.1 mL, 100 mmol) at 80° C. for 2 h. The mixture was cooled to room temperature and the precipitate was collected by filtration and dried under vacuum to provide the title compound (24 g, 97% yield). 1H NMR (300 MHz, CDCl3) δ 2.35-2.76 (m, 2 H), 2.80-3.11 (m, 2 H), 7.45-7.77 (m, 4 H), 8.55 (s, 1 H); MS (DCl/NH3) m/z 253 (M+H)+, 255 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07872010B2 |
| 出典データセット | uspto-grants-2011_01 |
| ORD ID | ord-0b8faecb9f0548448cc99ea7217a4202 |
| 出典メモ | uspto-grants-2011_01 |