関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 1-Chloro-2,6-dinitrobenzene | HCID 11814 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 4-Aminobenzene-1,3-diol hydrochloride | HCID 13408822 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-((2,6-Dinitrophenyl)amino)resorcinol | HCID 54063254 | 79.6% |
反応手順
6 g (30 mmol) of 1-chloro-2,6-dinitrobenzene and 4.8 g (30 mmol) of 4-aminoresorcinol hydrochloride were added to 300 ml of a mixture of tetrahydrofuran with dimethylformamide (1:1). After adding 7.8 g (60 mmol) of N,N-diisopropylethylamine thereto, the obtained mixture was stirred at room temperature for 24 hours. Then the solvent was distilled off under reduced pressure and the residue was dissolved in ethyl acetate and washed with a saturated aqueous solution of sodium chloride. Then it was dried over magnesium sulfate and concentrated and the residue was purified by silica gel column chromatography. Thus 6.95 g of 4-[(2,6-dinitrophenyl)amino]resorcinol was obtained. This product was dissolved in 125 ml of dimethylformamide and 25 ml of N,N-diisopropylethylamine was added thereto. After heating at 100° C. for 2 hours, the reaction mixture was concentrated and the residue was dissolved in ethyl acetate, washed with water, dried over magnesium sulfate and concentrated to dryness. Thus 5.4 g of the title compound was obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05846969 |
|---|
| 出典データセット | uspto-grants-1998_12 |
|---|
| ORD ID | ord-98a255e7e460486b95536713285ef828 |
|---|
| 出典メモ | uspto-grants-1998_12 |
|---|