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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1764129생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1764129

반응식

참여 물질

역할이름HCID투입량
반응물p-(1-Cyclooctenyl)-anisolHCID 284297—
반응물Pyridinium chlorideHCID 10176127—
용매WaterHCID 962—
생성물p-(1-Cyclooctenyl)-phenolHCID 53964233—

반응 조건

온도180 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04115416
출처 데이터셋uspto-grants-1978_09
ORD IDord-f746f2763f964198a8ba9a3117101512
출처 메모uspto-grants-1978_09