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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26384생성일: 2026년 10월 25일

Thionyl Chloride → Cyclohexanecarbonyl chloride, 5-methyl-2-(1-methylethyl)-

https://huagongshe.com/reaction/26384

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물p-Menthane-3-carboxylic acidHCID 97896—
생성물Cyclohexanecarbonyl chloride, 5-methyl-2-(1-methylethyl)-HCID 13734319—

반응 단계

p-Menthane-3-carboxylic acid (1.84g.), was heated under reflux with thionyl chloride (4 ml.) for 3 hours. The excess of thionyl chloride was then distilled off in vacuo. The crude produce p-menth-3-oyl chloride was dissolved in diethyl ether (25 ml.) and the ethereal solution was added with stirring and cooling to a solution of ethylamine (1.0 ml. of 70% w/s solution in water) and sodium hydroxide (0.4g.) in water (25 ml.). The mixture was stirred for one hour and the ethereal layer was then separated. The aqueous layer was washed with ether (25 ml.) and the combined ethereal solution was washed with dilute hydrochloric acid and then water. The ether solution was dried (MgSO4) and evaporated to give a white crystalline solid. The solid was recrystallised from acetone: water (9:1) by dissolving the crystals at room temperature and then cooling to produce N-ethyl-p-menthane-3-carboxamide as a white crystalline solid, mp. 82.5°-84.5°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04150052
출처 데이터셋uspto-grants-1979_04
ORD IDord-2685368400fd49bf850f29285e0c0a93
출처 메모uspto-grants-1979_04