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Acetic Anhydride → 1-(5-Bromo-3-methyl-1H-indazol-1-yl)ethan-1-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | Isoamyl Nitrite | HCID 8053 | — |
| 反応物 | 18-Crown-6 | HCID 28557 | — |
| 反応物 | Potassium Acetate | HCID 517044 | — |
| 反応物 | 4-Bromo-2-ethylaniline | HCID 2801283 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 1-(5-Bromo-3-methyl-1H-indazol-1-yl)ethan-1-one | HCID 59127382 | — |
反応手順
Acetic anhydride (4.73 ml) was added to the mixture of 4-bromo-2-ethylaniline (5.0 g) and KOAc (2.94 g) in CHCl3 (70 ml) and stirred for 30 minutes at reflux. Then isoamyl nitrite (6.65 ml) and 18-crown-6-ether (660 mg) was added to the reaction mixture and stirred for 12 h. under reflux. The reaction mixture was diluted with CHCl3, washed with water, and dried over sodium sulfate. After filtration and concentration, the residue was purified by silica gel chromatography (hexane/EtOAc), and crystallized from mixed solvent of hexane and CHCl3 to give intended compound as a yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08524730B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-7b5dffd064424629bd0d34f8d159136b |
| 出典メモ | uspto-grants-2013_09 |