関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethyl Carbonate | HCID 12021 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Methyl [p-(phenoxy)phenyl]acetate | HCID 12531834 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Dimethyl 2-(4-phenoxyphenyl)malonate | HCID 15540880 | 76.8% |
反応手順
To a suspension of NaH (1.02 g of 60% NaH in mineral oil washed with hexanes, 0.61 g, 25.6 mmol) in dry THF (30 mL) was added methyl (4-phenoxyphenyl)acetate (2.7 g, 11.1 mmol ) in dry THF (10 mL). The resulting mixture was stirred at room temperature for 30 minutes and then dimethylcarbonate (4.0 g, 3.75 mL, 44.4 mmol) was added . The reaction mixture was heated to reflux overnight and then cooled to room temperature, quenched with 1N HCl (60 mL), and extracted with ether (2×100 mL). The combined organic extracts were washed with water, then brine, dried (Na2SO4), concentrated, and purified using HPLC (porasil) eluted with 15% EtOAc/hexanes to give 2.56 g of dimethyl 2-(4-phenoxyphenyl)malonate as a white solid: 1H NMR (200 mHz, CDCl3) δ 7.39-6.92 (9H, m), 4.65 (1H, s), 3.75 (6H, s).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06265578B1 |
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| 出典データセット | uspto-grants-2001_07 |
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| ORD ID | ord-25a6cbcb2f6f4c4f92b12e3f6e0ac838 |
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| 出典メモ | uspto-grants-2001_07 |
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