戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1764129作成日:2026年10月26日

p-(1-Cyclooctenyl)-anisol → p-(1-Cyclooctenyl)-phenol

https://huagongshe.com/reaction/1764129

反応式

関与物質

役割名称HCID仕込み量
反応物p-(1-Cyclooctenyl)-anisolHCID 284297—
反応物Pyridinium chlorideHCID 10176127—
溶媒WaterHCID 962—
生成物p-(1-Cyclooctenyl)-phenolHCID 53964233—

反応条件

温度180 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04115416
出典データセットuspto-grants-1978_09
ORD IDord-f746f2763f964198a8ba9a3117101512
出典メモuspto-grants-1978_09