化工社化工社 化学情報印刷レポート · 研究参考用
Allyl bromide → 2-(Allyloxy)-1-bromo-5-methyl-3-nitrobenzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Allyl bromide | HCID 7841 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2-Bromo-4-methyl-6-nitrophenol | HCID 29918 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 2-(Allyloxy)-1-bromo-5-methyl-3-nitrobenzene | HCID 14977444 | 94.2% |
反応手順
To a mixture of 2-bromo-4-methyl-6-nitrophenol (7.00 g, 30.2 mmol), K2CO3 (6.26 g, 45.3 mmol) in acetone (105 mL) was added allyl bromide (3.80 ml, 45.3 mmol). The reaction mixture was stirred at room temperature overnight. It was then heated at 40° C. for 5 hrs. Inorganic salts were filtered and washed with acetone. The filtrate was concentrated to give 7.74 g (94%) of the desired product. MS (DCI/NH3) m/z: 289.0 (M+NH4)+; 1H NMR (300 MHz, CD3OD) δ ppm 2.37 (s, 3 H) 4.61 (d, J=6.10 Hz, 2 H) 5.26 (dd, J=10.51, 1.80 Hz, 1 H) 5.39 (dd, J=17.29, 1.80 Hz, 1 H) 6.09 (m, 1 H) 7.63 (s, 1 H) 7.74 (s, 1 H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07163939B2 |
| 出典データセット | uspto-grants-2007_01 |
| ORD ID | ord-45249ef8d80d45258c2767c58c8dce87 |
| 出典メモ | uspto-grants-2007_01 |