関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Methyl 4-cyano-3-(p-fluorophenyl)-4-(m-fluorophenyl)butyrate | HCID 14838737 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 4-Cyano-3-(4-fluorophenyl)-4-(3-fluorophenyl)butanoic acid | HCID 14838739 | — |
反応手順
Under protective gas (Ar), 10 ml of 2 molar aqueous sodium hydroxide solution were added to 1.75 g (5.55 mmol) of methyl 4-cyano-3-(4-fluorophenyl)-4-(3-fluorophenyl)butanoate (Example A1) in 50.0 ml of methanol, and the mixture was stirred at 25° C. for 8 h. The methanol was removed under reduced pressure. The residue was acidified with concentrated hydrochloric acid (pH=3) and extracted three times with in each case 15 ml of dichloromethane. The combined organic phases were dried over sodium sulphate and the solvent was removed under reduced pressure. This gave 1.62 g (96.9% of theory) of the title compound in the form of colourless crystals (erythro:threo=49:51 according to comparison of the multiplets in the 1H-NMR in CDCl3 at 2.60 and 2.85 ppm).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09084425B2 |
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| 出典データセット | uspto-grants-2015_07 |
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| ORD ID | ord-dbb67efb1c9f4b1f9a729e1a689a5507 |
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| 出典メモ | uspto-grants-2015_07 |
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