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Triethylamine → 2-(2,4-Dinitrophenoxy)-1H-isoindole-1,3(2H)-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | N-Hydroxyphthalimide | HCID 10665 | — |
| 反応物 | 1-Bromo-2,4-dinitrobenzene | HCID 11441 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 2-(2,4-Dinitrophenoxy)-1H-isoindole-1,3(2H)-dione | HCID 7036309 | 96.4% |
反応手順
To a suspension of 2-hydroxyisoindoline-1,3-dione (20.0 g, 0.12 mol) in acetone (400 mL) was added Et3N (14.9 g, 0.15 mol), the mixture was stirred at room temperature until it became a homogeneous solution, then 1-bromo-2,4-dinitrobenzene Y-1 (30.2 g, 0.12 mol) was added. The reaction was stirred at room temperature for 3 h, then poured into ice-water, the resulting precipitate was filtered and washed three times with cold MeOH, dried in vacuum to afford the title compound (38.1 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08987269B2 |
| 出典データセット | uspto-grants-2015_03 |
| ORD ID | ord-dbb3f970c0724ff3a7a479fecd60add1 |
| 出典メモ | uspto-grants-2015_03 |