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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1198456생성일: 2026년 10월 27일

2-Aminophenol → 2-(4-chlorophenyl)-3-oxo 3,4-dihyro-2H-1,4-benzoxazine

https://huagongshe.com/reaction/1198456

반응식

참여 물질

역할이름HCID투입량
반응물2-AminophenolHCID 5801—
반응물Sodium BicarbonateHCID 516892—
반응물Bromo-4-chlorophenylacetyl chlorideHCID 12575778—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물2-(4-chlorophenyl)-3-oxo 3,4-dihyro-2H-1,4-benzoxazineHCID 1084889776.9%

반응 단계

To a solution of 2-aminophenol (13.5 g) in ethyl acetate (150 ml) is added a solution of sodium hydrogen carbonate (15 g) in water (300 ml), and to the mixture is added dropwise a solution of α -bromo-4-chlorophenylacetyl chloride (32.2 g) in toluene with vigorous stirring under ice cooling. After the mixture is stirred at room temperature for one hour, the solvent in the organic layer is distilled off and the residue is dissolved in acetone. To the solution is added potassium carbonate (20 g), and the mixture is stirred at room temperature overnight. The solvent is distilled off and to the residue is added water. The mixture is extracted with ethyl acetate. The ethyl acetate layer is washed, dried and distilled to remove the solvent, and the residue is recrystallized from ethyl acetate-n-hexane to give 2-(4-chlorophenyl)-3-oxo 3,4-dihyro-2H-1,4-benzoxazine (24.0 g) as crystals. M.p. 180.5°-181.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05281592
출처 데이터셋uspto-grants-1994_01
ORD IDord-267574ecad19420bb0f49d0aefa2077c
출처 메모uspto-grants-1994_01