関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diethyl Malonate | HCID 7761 | — |
| 反応物 | Magnesium Chloride | HCID 5360315 | — |
| 反応物 | 2-(4-Fluorophenyl)-2-methylpropanoic acid | HCID 20163803 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 溶媒 | Thionyl Chloride | HCID 24386 | — |
| 生成物 | Diethyl 2-(2-(4-fluorophenyl)-2-methylpropanoyl)malonate | HCID 67099824 | 96.3% |
反応手順
A mixture of diethyl malonate (3 g, 16 mmol) in 50 mL ACN was stirred at 0° C., was treated with MgCl2 (2 g, 18 mmol) in one portion, and was treated dropwise with TEA (3 g, 33 mmol). The mixture was stirred at room temperature for 2.5 hours. A mixture of 2-(4-fluorophenyl)-2-methylpropanoic acid (3 g, 16 mmol) in thionyl chloride (20 mL) was refluxed for 2 hours and then concentrated in vacuo. The residue was diluted with 10 mL ACN, and was added dropwise to the above mixture. The mixture was stirred at 50° C. for 15 hours. The resulting mixture was then cooled to room temperature, diluted with 100 mL ether, washed with H2O (2×50 mL) and brine 20 mL, dried over anhydrous Na2SO4, and concentrated in vacuo. The crude product was purified by column chromatography eluting with 10-20% EtOAc/hexane to give 5 g of the product as pale yellow oil. MS m/e=325 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07928139B2 |
|---|
| 出典データセット | uspto-grants-2011_04 |
|---|
| ORD ID | ord-18c0cb6cc0984bc99a5effa35e620067 |
|---|
| 出典メモ | uspto-grants-2011_04 |
|---|