関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Propanoic acid, 2-bromo-2-methyl-, ethyl ester | HCID 11745 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2-(4-Bromophenyl)ethanol | HCID 72851 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Ethyl 2-[2-(4-bromophenyl)ethoxy]-2-methylpropionate | HCID 59792867 | 15.2% |
反応手順
To a solution of 2-(4-bromophenyl)ethanol (1 g, 5 mmol) in THF (15 ml) was added sodium hydride (60% in parafin liquid) (220 mg, 5.5 mmol) at 0° C., and the mixture was stirred at room temperature for 15 minutes. To the mixture was added ethyl 2-bromoisobutyrate (1.08 g, 5.5 mmol), and the mixture was stirred at room temperature for 12 hours. To this reaction solution were added ethyl acetate and a saturated aqueous ammonium chloride solution, and the organic layer was separated. The aqueous layer was extracted twice with ethyl acetate, and the extracts were combined with the organic layer. The organic layer was collected, dried over anhydrous sodium sulfate, filtered, and the solvent was evaporated under reduced pressure. The resultant was purified by silica gel column chromatography (hexane:ethyl acetate=10:1) to give the title compound (240 mg, 15%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07425642B2 |
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| 出典データセット | uspto-grants-2008_09 |
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| ORD ID | ord-f165681782f44475b0ce8dcc89e8ab70 |
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| 出典メモ | uspto-grants-2008_09 |
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