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Hydrogen Bromide → 2-Bromo-1-(4-methylthiazol-5-yl)ethanone hydrobromide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrogen Bromide | HCID 260 | — |
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | 5-Acetyl-4-methylthiazole | HCID 162292 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 2-Bromo-1-(4-methylthiazol-5-yl)ethanone hydrobromide | HCID 131735473 | 74.5% |
反応手順
220 mg (1.56 mmol) of 1-(4-methylthiazol-5-yl)ethanone are dissolved in 10 mL of glacial acetic acid. 769 μl (4.67 mmol) of hydrobromic acid and 88 μl (1.71 mmol) of bromine are added to the medium. The reaction mixture is placed under magnetic stirring at room temperature for 2 hours. Ethyl ether is added to the solution until a precipitate appears. The precipitate corresponding to 2-bromo-1-(4-methylthiazol-5-yl)ethanone hydrobromide is filtered off, washed with ethyl ether and dried. The 350 mg of product obtained have the following characteristics:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09321790B2 |
| 出典データセット | uspto-grants-2016_04 |
| ORD ID | ord-44d8cd39d53b4e44a88f58b454fa5c87 |
| 出典メモ | uspto-grants-2016_04 |