関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Rofecoxib | HCID 5090 | — |
| 反応物 | Diisobutylaluminum hydride | HCID 14487 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diol | HCID 57434773 | 98.7% |
反応手順
To a solution of 110 g of 4-(4-methanesulfonyl-phenyl)-3-phenyl-5H-furan-2-one in 1.5 L of dichloromethane stirred at −78° C., 150 mL of DIBAL was added dropwise. The resulting mixture was warmed to room temperature and stirred overnight. The reaction mixture was then cooled to −78° C., and 1.2 L of 1 M aqueous NaOH was added dropwise. After the addition, the resulting mixture was warmed to room temperature and the organic phase was separated. The aqueous phase was extracted with dichloromethane. The organic phases were combined and dried over Na2SO4. 110 g of the titled compound was obtained after evaporation. 1H NMR (acetone-d6, 500 M Hz): δ 7.69 (d, 2H), 7.36 (d, 2H), 7.16–7.05 (m, 5H), 4.66 (d, 2H), 4.63 (d, 2H), 4.19 (t, 1H, OH), 4.17 (t, 1 H. OH), 3.04 (s, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07169809B2 |
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| 出典データセット | uspto-grants-2007_01 |
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| ORD ID | ord-5edd1a315fdf4ebbb46c36c2676df4c7 |
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| 出典メモ | uspto-grants-2007_01 |
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