関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | p-(1-Cyclooctenyl)-anisol | HCID 284297 | — |
| 反応物 | Pyridinium chloride | HCID 10176127 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | p-(1-Cyclooctenyl)-phenol | HCID 53964233 | — |
反応手順
80 Grams of p-(1-cyclooctenyl)-anisol and 175 g of pyridine-hydrochloride are thoroughly mixed and heated for 4 hours under nitrogen to 180° C. The mixture is cooled, treated with water and extracted with benzene. The benzene extracts are shaken with 3×100 ml of N-sodium hydroxide solution. The alkaline phase is acidified with 2N hydrochloric acid and extracted with ether. The ether solution is dried over sodium sulphate and evaporated. The residue is recrystallised from benzene-petroleum ether to yield the p-(1-cyclooctenyl)-phenol (m.p. 95°-97° C).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04115416 |
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| 出典データセット | uspto-grants-1978_09 |
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| ORD ID | ord-f746f2763f964198a8ba9a3117101512 |
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| 出典メモ | uspto-grants-1978_09 |
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