Sulfuric Acid → Methyl 2-amino-4-chloro-5-nitrobenzoate
反応式
[CH3:1][O:2][C:3](=[O:18])[C:4]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[C:7]([Cl:13])=[CH:6][C:5]=1[NH:14]C(=O)C.S(=O)(=O)(O)O>>[CH3:1][O:2][C:3](=[O:18])[C:4]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[C:7]([Cl:13])=[CH:6][C:5]=1[NH2:14]参加物
3
実験手順
To a solution of 2-acetylamino-4-chloro-5-nitrobenzoic acid methyl ester (1.02 g in 15 mL methanol) was added 1 mL of conc. sulfuric acid and the mixture heated to reflux on an oil bath. After 1 hour, the mixture was concentrated in vacuo and the resulting solid dissolved in 200 mL ethyl acetate. This was then washed with 10% sodium bicarbonate (2×100 mL) and brine (100 mL) and the organics dried over magnesium sulfate. The concentrate was recrystallized from methanol to give the title compound (0.82 g).
後処理
- temperaturethe mixture heated
- temperatureto reflux on an oil bath
- concentrationthe mixture was concentrated in vacuo
- dissolutionthe resulting solid dissolved in 200 mL ethyl acetate
- washThis was then washed with 10% sodium bicarbonate (2×100 mL) and brine (100 mL)
- dry with materialthe organics dried over magnesium sulfate
- customThe concentrate was recrystallized from methanol
出典と根拠
- ORDレコード
- ord-91e5a302a6c846f68d59165c6c407441
- 出典データセット
- uspto-grants-2000_11
- 特許番号
- US06147088
反応ノート
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