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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 234899생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/234899

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물2-Bromobutanoyl bromideHCID 117293—
반응물Sodium BicarbonateHCID 516892—
반응물Benzoic acid, 4-amino-3-hydroxy-, methyl esterHCID 7020619—
용매WaterHCID 962—
생성물2-ethyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazineHCID 2335316487%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05597820
출처 데이터셋uspto-grants-1997_01
ORD IDord-3f799eee7bde4f37b8c1e0686a48f40d
출처 메모uspto-grants-1997_01