関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 3-(4-(Trifluoromethyl)benzamido)propyloxyphenyl benzoate | HCID 86754495 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 3-(4-(Trifluoromethyl)benzamido)propyloxyphenol | HCID 86754494 | 94% |
反応手順
To a mixture of 0.87 g of 3-ethyl-5-methyl-4-(3-(4-(trifluoromethyl)benzamido)propyloxyphenyl benzoate and 10 ml of methanol was added a mixture of 0.16 g of sodium hydroxide and 2 m of water, while stirring at 0° C. After stirring at room temperature for 24 hours, the reaction mixture was made weak acidic by the addition of 10% hydrochloric acid, and extracted with 50 ml of ethyl acetate. The ethyl acetate layer was washed with saturated saline solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure to give a residue. The residue was subjected to silica gel chromatography, which afforded 0.66 g of 3-ethyl-5-methyl-4-(3-(4-(trifluoromethyl)benzamido)propyloxyphenol (94% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06214835B1 |
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| 出典データセット | uspto-grants-2001_04 |
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| ORD ID | ord-cdf1e3aa33c043e3ade040d9bac596ec |
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| 出典メモ | uspto-grants-2001_04 |
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