化工社化工社 化学情報印刷レポート · 研究参考用
1,2-Dichloroethane → (4-Bromo-3-fluorophenyl)(morpholin-4-yl)methanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,2-Dichloroethane | HCID 11 | — |
| 反応物 | Ethylmorpholine | HCID 7525 | — |
| 反応物 | Morpholine | HCID 8083 | — |
| 反応物 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 反応物 | 4-Bromo-3-fluorobenzoic acid | HCID 2773341 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (4-Bromo-3-fluorophenyl)(morpholin-4-yl)methanone | HCID 48474115 | 98.5% |
反応手順
A 500 mL flask was charged with 4-bromo-3-fluorobenzoic acid (5.00 g, 22.83 mmol), 100 mL DMF, morpholine (2.4 ml, 27.5 mmol), and 4-Ethylmorpholine (8.6 ml, 67.9 mmol). HOBt (4.32 g, 32.0 mmol) was added followed by EDC (5.25 g, 27.4 mmol) and the reaction allowed to stir at room temperature for 18 hours. The reaction was concentrated and the resulting orange syrup taken up in 100 mL EtOAc and 100 mL water. The organic layer was washed with 100 mL 2N HCl, 100 mL saturated sodium bicarbonate, and 100 mL saturated sodium chloride. The organic was then dried with MgSO4, filtered, and concentrated to give 6.476 g (98%) of a viscous yellow oil. This material was used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08236799B2 |
| 出典データセット | uspto-grants-2012_08 |
| ORD ID | ord-77d51c2daee940da81507bf578f69cff |
| 出典メモ | uspto-grants-2012_08 |