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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 258636생성일: 2026년 10월 26일

Acetic Acid → 2,4-Dihydroxy-4b,6,7,8,8a,10-hexahydrophenanthren-9(5H)-one

https://huagongshe.com/reaction/258636

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물PhloroglucinolHCID 359—
반응물1-AcetylcyclohexeneHCID 13612—
반응물Potassium HydroxideHCID 14797—
용매2-MethoxyethanolHCID 8019—
용매Ethyl AcetateHCID 8857—
생성물2,4-Dihydroxy-4b,6,7,8,8a,10-hexahydrophenanthren-9(5H)-oneHCID 20322774—

반응 조건

온도140 °C

반응 단계

To a flask equipped with a stirrer, dropping funnel, condenser and gas inlet tube maintained under a nitrogen atmosphere, there is added 50 g. (0.89) moles of potassium hydroxide in one liter of 2-methoxyethanol. Stirring is initiated and 100 g. (0.79 mole) of anhydrous phloroglucinol is added in three portions, followed by the addition of 100 g. (0.80 mole) of 1-acetyl-cyclohexene while maintaining the temperature at 50° C. The resulting solution is refluxed at 140° C. for 4 hours. After cooling there is then added gradually 53.6 g. of acetic acid while obtaining a pH of approximately 7. The solvent is then removed in vacuo, and the residue is further heated in an oil bath at 70° C., to obtain a viscous residue. The resulting residue is dissolved in ethyl acetate and water washed twice with water, dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to obtain a brown solid. The resulting solid is recrystallized from ethyl acetate/cyclohexane to give 2,4-dihydroxy-4b,5,6,7,8,8a,9,10-octahydro-9-oxo-phenanthrene; m.p. 220°-223° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04034045
출처 데이터셋uspto-grants-1977_07
ORD IDord-62fd1dc90f0243119c29b2b0a50756aa
출처 메모uspto-grants-1977_07