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Ethanol → Ethyl 4-(2-aminophenyl)-4-oxobutanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | 2-Amino-gamma-oxobenzenebutanoic acid | HCID 6420149 | — |
| 生成物 | Ethyl 4-(2-aminophenyl)-4-oxobutanoate | HCID 21283602 | — |
反応手順
3-(2-Aminobenzoyl)propionic acid (26.7 g) and concentrated sulphuric acid (25 cc) in absolute ethanol (250 cc) are stirred for 17 hours at room temperature (approximately 20° C.). The ethanol is evaporated off under reduced pressure, water (200 cc) and ethyl acetate (200 cc) are added and potassium carbonate is added until the pH is 8. The mixture is filtered, and the aqueous phase decanted and re-extracted with ethyl acetate (2×100 cc). The organic phase is dried over magnesium sulphate, filtered and evaporated to dryness under reduced pressure. Ethyl 3-(2-aminobenzoyl)propionate (24.8 g) is obtained in the form of an oil. The proton NMR spectrum in deuterated chloroform shows the following characteristics:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04788199 |
| 出典データセット | uspto-grants-1988_11 |
| ORD ID | ord-2dc62d66979b46ea86296f21d8bf4c31 |
| 出典メモ | uspto-grants-1988_11 |