関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Nitroethane | HCID 6587 | — |
| 反応物 | Di-tert-butyl dicarbonate | HCID 90495 | — |
| 反応物 | 4-Ethynyl-3-methyl-benzofuran-2-carboxylic acid ethyl ester | HCID 86058915 | — |
| 触媒 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 3-Methyl-4-(3-methyl-isoxazol-5-yl)-benzofuran-2-carboxylic acid ethyl ester | HCID 68714707 | 25% |
反応手順
To a solution of 4-ethynyl-3-methyl-benzofuran-2-carboxylic acid ethyl ester (228 mg, 0.99 mmol, 1 eq.) in acetonitrile (5 mL) under argon, was added di-tert-butyl dicarbonate (327 mg, 1.5 mmol, 1.5 eq.), and 4-(dimethylamino)pyridine (12 mg, 0.1 mmol, 0.1 eq.). Nitroethane (79 uL, 1.1 mmol, and 1.1 eq.) in acetonitrile (5 mL) was added drop-wise to the reaction mixture, and the reaction was stirred at room temperature for 72 hours. After work-up and flash column chromatography, 3-methyl-4-(3-methyl-isoxazol-5-yl)-benzofuran-2-carboxylic acid ethyl ester was obtained in 25% yield. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.4 (t, J=7.1 Hz, 3 H) 2.3 (s, 3 H) 2.4 (s, 3 H) 4.4 (q, J=7.1 Hz, 2 H) 6.8 (s, 1 H) 7.5 (dd, J=7.5, 0.9 Hz, 1 H) 7.6 (m, 1 H) 7.9 (dd, J=8.5, 0.9 Hz, 1 H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07420001B2 |
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| 出典データセット | uspto-grants-2008_09 |
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| ORD ID | ord-3f44d056d2ef4778a58629bd5e844bbb |
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| 出典メモ | uspto-grants-2008_09 |
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