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N,N-Dimethylaniline → 1H-naphth(2,1-b)(1,4)oxazin-2(3H)-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N,N-Dimethylaniline | HCID 949 | — |
| 反応物 | Chloroacetyl chloride | HCID 6577 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 1-Amino-2-naphthol | HCID 14535 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 1H-naphth(2,1-b)(1,4)oxazin-2(3H)-one | HCID 84665 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05246929 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-cda7d710b0294e50b3206a6efffce4f5 |
| 出典メモ | uspto-grants-1993_09 |