関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | Benzene, 1-bromo-3-iodo- | HCID 11561 | — |
| 反応物 | 2,2,6,6-Tetramethyl-3,5-heptanedione | HCID 70700 | — |
| 反応物 | Methyl 3-(4-Hydroxy-2-methylphenyl)propanoate | HCID 13551833 | — |
| 触媒 | Cuprous chloride | HCID 62652 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | 3-[4-(3-Bromo-phenoxy)-2-methyl-phenyl]-propionic acid methyl ester | HCID 57894192 | 60% |
反応手順
A mixture of 3-(4-hydroxy-2-methyl-phenyl)-propionic acid methyl ester (4.0 g, 20.6 mmol), 1-bromo-3-iodobenzene (17.49 g, 61.8 mmol), cesium carbonate (8.05 g, 24.7 mmol), copper (I) chloride (1.02 g, 10.3 mmol) and 2,2,6,6-tetramethyl-3,5-heptanedione (0.95 g, 5.15 mmol) in 1-methyl-2-pyrrolidinone (40 mL) is heated to 120° C. for 17 hours under N2. The reaction is cooled and quenched with 1 N HCl (50 mL). The mixture is then diluted with Et2O and extracted with water. The organic layer is dried (Na2SO4), and the solvent is removed in vacuo to afford crude product that is absorbed on silica gel and purified by flash chromatography using 9/1 hexanes/ethyl acetate to afford 4.30 g (60%) of the title compound. Rf=0.33 (4/1 hexanes/EtOAc). 1H NMR (400 MHz, CDCl3); MS (ES+) m/z mass calculated for C17H17O3Br 348, found 349 and 351 (M+1 and M+3, 100%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07608639B2 |
|---|
| 出典データセット | uspto-grants-2009_10 |
|---|
| ORD ID | ord-50ada645cd54442197b4edc8fc39a3e6 |
|---|
| 出典メモ | uspto-grants-2009_10 |
|---|