関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| 反応物 | 4-Methoxy-3-methylphenol | HCID 297394 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Acrylonitrile | HCID 7855 | — |
| 生成物 | 3-(4-Methoxy-3-methylphenoxy)propanenitrile | HCID 67530876 | — |
反応手順
A solution of 7.0 grams (0.050 mole) of 3-methyl-4-methoxyphenol (known compound) in 20 mL of acrylonitrile was stirred, and 0.4 mL of benzyltrimethylammonium hydroxide (Triton® B) was added. Upon completion of addition, the reaction mixture was warmed to reflux where it stirred during a 21 hour period. The reaction mixture was then cooled to ambient temperature and diluted with 100 mL of diethyl ether. The mixture was then first washed with three 50 mL portions of an aqueous solution of 10% potassium hydroxide, then with three 50 mL portions of aqueous 4N hydrochloric acid. The organic layer was dried with sodium sulfate, and the mixture was filtered. The filtrate was concentrated under reduced pressure, yielding 6.0 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07417057B2 |
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| 出典データセット | uspto-grants-2008_08 |
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| ORD ID | ord-2e587dcba0a4437ebf471affba0dc864 |
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| 出典メモ | uspto-grants-2008_08 |
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