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Benzyl Bromide → Ethyl 2-(4-(benzyloxy)-3-bromophenyl)acetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzyl Bromide | HCID 7498 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | Ethyl 2-(3-bromo-4-hydroxyphenyl)acetate | HCID 18620106 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | Ethyl 2-(4-(benzyloxy)-3-bromophenyl)acetate | HCID 18620085 | — |
反応手順
To a suspension of (3-bromo-4-hydroxy-phenyl)-acetic acid ethyl ester (0.100 g, 0.39 mmol) and cesium carbonate (0.376 g, 1.16 mmol) in MeCN was added benzyl bromide (0.06 mL, 0.46 mmol), and the reaction was stirred at room temperature until no starting material was seen by analytical tlc. The mixture was partitioned between EtOAc and H2O, and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered, and concentrated to give the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08067445B2 |
| 出典データセット | uspto-grants-2011_11 |
| ORD ID | ord-3a0aa6086fd9412c80c875c8103a2250 |
| 出典メモ | uspto-grants-2011_11 |