関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | Isoamyl Nitrite | HCID 8053 | — |
| 反応物 | Phosphinic Acid | HCID 4124402 | — |
| 反応物 | Ethyl 2-amino-3-bromo-5-methylbenzoate | HCID 54594338 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Ethyl 3-bromo-5-methylbenzoate | HCID 20086624 | 87.3% |
反応手順
Ethanol (20 mL) was added to ethyl 2-amino-3-bromo-5-methylbenzoate obtained in Example (259d) (715 mg, 2.8 mmol). While the mixture was stirred, trifluoroacetic acid (0.82 mL, 11.1 mmol), isopentyl nitrite (649 mg, 5.5 mmol) and hypophosphorous acid (7.3 g, 55.4 mmol) were added under ice-cooling, followed by stirring at room temperature for 30 minutes. The reaction solution was diluted and extracted with ethyl acetate and aqueous sodium bicarbonate solution. The organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane=0/10, 2/8) to obtain 594 mg of the title compound as a light yellow oily substance (88%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US08536197B2 |
|---|
| 出典データセット | uspto-grants-2013_09 |
|---|
| ORD ID | ord-c872ad6b93844f3591336c2f063f31e6 |
|---|
| 出典メモ | uspto-grants-2013_09 |
|---|