化工社化工社 化学情報印刷レポート · 研究参考用
Sodium Iodide → Methyl 3-(2-(benzyloxy)-5-bromophenyl)-3-phenylpropanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Iodide | HCID 5238 | — |
| 反応物 | Benzyl Chloride | HCID 7503 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 6-Bromo-3,4-dihydro-4-phenyl-2H-1-benzopyran-2-one | HCID 2924973 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Methyl 3-(2-(benzyloxy)-5-bromophenyl)-3-phenylpropanoate | HCID 21476697 | 102.9% |
反応手順
6-Bromo-4-phenyl-3,4-dihydro-coumarine (290 g, 0.96 mole) was dissolved in a mixture of methanol (1 L) and acetone (1 L). To the above solution were added potassium carbonate (160 g, 1.16 mole), α-chlorotoluene (140 g, 1.1 mole) and sodium iodide (30 g, 0.47 mole), and the mixture was stirred under reflux for 3 h. The solution was concentrated by distillation, and the residue treated with water and extracted with diethyl ether. The ethereal layer was washed with water, saturated sodium carbonate solution and water, successively. The organic layer was dried over sodium sulfate, filtered and then evaporated to give 420 g (≈100%) of the title compound as a light yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | USRE040851E1 |
| 出典データセット | uspto-grants-2009_07 |
| ORD ID | ord-7f6db4f2f8654539bef679b64303df3a |
| 出典メモ | uspto-grants-2009_07 |