Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N,N-Dimethylaniline → 1H-naphth(2,1-b)(1,4)oxazin-2(3H)-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N,N-Dimethylaniline | HCID 949 | — |
| 반응물 | Chloroacetyl chloride | HCID 6577 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 1-Amino-2-naphthol | HCID 14535 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 1H-naphth(2,1-b)(1,4)oxazin-2(3H)-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05246929 |
| 출처 데이터셋 | uspto-grants-1993_09 |
| ORD ID | ord-cda7d710b0294e50b3206a6efffce4f5 |
| 출처 메모 | uspto-grants-1993_09 |