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HRID 5829생성일: 2026년 10월 23일

N,N-Dimethylaniline → 3-(4-chlorophenyl)-1H-naphtho[2,1-b][1,4]oxazin-2(3H)-one

https://huagongshe.com/ko/reaction/5829

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물TetrahydrofuranHCID 8028—
반응물1-Amino-2-naphtholHCID 14535—
반응물Bromo-4-chlorophenylacetyl chlorideHCID 12575778—
용매Ethyl AcetateHCID 8857—
생성물3-(4-chlorophenyl)-1H-naphtho[2,1-b][1,4]oxazin-2(3H)-oneHCID 1898444272.8%

반응 단계

To a mixture of 1-amino-2-naphthol (9.4 g), N,N-dimethylaniline (17.87 g) and tetrahydrofuran (160 ml) is added dropwise α-bromo-4-chlorophenylacetyl chloride (18.97 g) under ice cooling, and the mixture is stirred for one hour. To the reaction mixture is added ethyl acetate, and the ethyl acetate layer is washed, dried and distilled to remove the solvent. The resulting oil is dissolved in acetone (500 ml) and thereto is added potassium carbonate (40.8 g), and the mixture is refluxed for 2 hours, and acetone is distilled off. To the residue is added water, and the precipitate is separated by filtration, washed, dried and recrystallized from tetrahyrofuran to give 3-(4-chlorophenyl)-1H-naphtho[2,1-b][1,4]oxazin-2(3H)-one (13.29 g, yield 72.8%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246929
출처 데이터셋uspto-grants-1993_09
ORD IDord-d364fc4681ef4cc7a031ee2d8b2fe643
출처 메모uspto-grants-1993_09