関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 1-Chloroethan-1-ol | HCID 12639035 | — |
| 反応物 | 4-hydroxy-3-methyl-N-(1-propyl-butyl)-benzamide | HCID 57527768 | — |
| 生成物 | N-(heptan-4-yl)-4-(2-methoxyethoxy)-3-methylbenzamide | HCID 57527906 | 39% |
反応手順
Potassium hydroxide (4 mmol) was dissolved in ethanol (5 mL) and heated at 80° C. 4-hydroxy-3-methyl-N-(1-propyl-butyl)-benzamide (example 58) (1 mmol) was added into the solution followed by chloroethanol (3 mmol). The reaction was stirred overnight at 80° C. The reaction mixture was concentrated down and dissolved in 5% citric acid. The mixture was stirred for 1 hour. The aqueous mixture was extracted three times with ethyl acetate. The combined ethyl acetate was washed with water and dried down over sodium sulfate. The organic layer was concentrated down and purified by HPLC to yield 39% of N-(heptan-4-yl)-4-(2-methoxyethoxy)-3-methylbenzamide. MS (M+H, 308.25).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08895050B2 |
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| 出典データセット | uspto-grants-2014_11 |
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| ORD ID | ord-57afbe97652f466dbe71c191c0288561 |
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| 出典メモ | uspto-grants-2014_11 |
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