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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1439857생성일: 2026년 10월 27일

N,N-Dimethylaniline → 1H-naphth(2,1-b)(1,4)oxazin-2(3H)-one

https://huagongshe.com/reaction/1439857

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물Chloroacetyl chlorideHCID 6577—
반응물TetrahydrofuranHCID 8028—
반응물1-Amino-2-naphtholHCID 14535—
용매Ethyl AcetateHCID 8857—
생성물1H-naphth(2,1-b)(1,4)oxazin-2(3H)-oneHCID 84665—

반응 단계

To a mixture of 1-amino-2-naphthol (16.9 g), N,N-dimethylaniline (19.3 g) and tetrahydrofuran (200 ml) is added dropwise chloroacetyl chloride under ice cooling, and the mixture is stirred at the same temperature 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 (75 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 1H-naphtho[2,1-b][1,4]oxazin-2(3H)-one (13.1 g). M.p. 219°-220.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05496815
출처 데이터셋uspto-grants-1996_03
ORD IDord-612c7cbaea9e4c7b8d1d681e848412e0
출처 메모uspto-grants-1996_03