関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Ethyl 4-(2',3'-dimethoxyphenyl)-3-phenylbutyrate | HCID 19961164 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 4-(2',3'-Dimethoxyphenyl) 3-phenylbutyric acid | HCID 12478543 | 100.2% |
反応手順
Ethyl 4-(2',3'-dimethoxyphenyl)-3-phenylbutyrate (40.3 g, 123 mmol), from Step 3, was dissolved in 400 mL of methanol and 62 mL of 3M aqueous sodium hydroxide solution was added in one portion. The reaction mixture was stirred at ambient temperature for 18 h. The reaction mixture was concentrated and the residue was partitioned between 300 mL of diethyl ether and 200 mL of water. The layers were separated and the aqueous layer was adjusted to pH 6 with 6M aqueous hydrochloric acid solution and extracted with 3×200 mL of diethyl ether. The organic layers were combined, washed with brine, dried over anhydrous magnesium sulfate, faltered and concentrated in vacuo to give 37 g (100% yield) of the title compound as a colorless oil. The 1H NMR spectrum was identical to the spectrum reported for the product of Step 5 of Method A, Example 1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05621133 |
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| 出典データセット | uspto-grants-1997_04 |
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| ORD ID | ord-977908a01ff54d448822db6a60e9a34a |
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| 出典メモ | uspto-grants-1997_04 |
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