戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 234899作成日:2026年10月27日

Ethyl Acetate → 2-ethyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine

https://huagongshe.com/reaction/234899

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物2-Bromobutanoyl bromideHCID 117293—
反応物Sodium BicarbonateHCID 516892—
反応物Benzoic acid, 4-amino-3-hydroxy-, methyl esterHCID 7020619—
溶媒WaterHCID 962—
生成物2-ethyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazineHCID 2335316487%

反応手順

To a solution of 2-amino-5-methoxycarbonylphenol [Tetrahedron, 46(15), 5177-5186 (1990)] (9.80 g) in a mixed solvent of ethyl acetate (200 ml) and water (200 ml) were added sodium hydrogen carbonate (7.30 g) and 2-bromobutyryl bromide (13.70 g) and the mixture was stirred at room temperature for 10 minutes. The organic layer was separated and the solvent was distilled off under reduced pressure. The resulting residue was dissolved in dimethylformamide (500 ml), to the solution was added potassium carbonate (8.90 g) and the mixture was stirred at room temperature for a day. The reaction solution was poured into water to give precipitates, which were taken by filtration and dried to give 2-ethyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (12.0 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05597820
出典データセットuspto-grants-1997_01
ORD IDord-3f799eee7bde4f37b8c1e0686a48f40d
出典メモuspto-grants-1997_01