돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5845생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/5845

반응식

참여 물질

역할이름HCID투입량
반응물2-AminophenolHCID 5801—
반응물Sodium BicarbonateHCID 516892—
반응물2-Bromo-p-chlorophenylacetyl chlorideHCID 19794234—
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 o-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 번호US05246929
출처 데이터셋uspto-grants-1993_09
ORD IDord-ffca69bda88f4569b98eca5bd5ca7c45
출처 메모uspto-grants-1993_09