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Ammonium Hydroxide → 7-Methoxy-2,6-dimethylquinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonium Hydroxide | HCID 14923 | — |
| 反応物 | 3-Methoxy-4-methylaniline | HCID 27882 | — |
| 反応物 | Crotonaldehyde | HCID 447466 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 生成物 | 7-Methoxy-2,6-dimethylquinoline | HCID 86707471 | 42.5% |
反応手順
To 3-methoxy-4-methylaniline (1.0 g, 7.29 mmol) in refluxing in 6N HCl (50 mL) was added dropwise (E)-but-2-enal (1.02 g, 14.6 mmol). The reaction was heated to reflux for 2 hours then cooled down and neutralized with NH4OH. The organic phase was extracted with DCM and the combined organic phases dried over MgSO4, filtered and concentrated under reduced pressure to leave a dark residue. The residue was purified by reverse phase chromatography (SP4, 25M, eluting with a gradient of water/ACN 100:0 to 0:100, 20 column volumes) to yield 7-methoxy-2,6-dimethylquinoline (580 mg, 29.7% yield) as a beige solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08889704B2 |
| 出典データセット | uspto-grants-2014_11 |
| ORD ID | ord-d1a62e775ff14853b31c0c1618bab9fe |
| 出典メモ | uspto-grants-2014_11 |