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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1743344생성일: 2026년 10월 25일

Hydrochloric Acid → 2-(9-Fluorenon-4-yl)hydroxychromone

https://huagongshe.com/reaction/1743344

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Lithium HydroxideHCID 3939—
반응물2',4'-DihydroxyacetophenoneHCID 6990—
반응물9-Fluorenone-4-carbonyl chlorideHCID 610142—
용매TetrahydrofuranHCID 8028—
생성물2-(9-Fluorenon-4-yl)hydroxychromoneHCID 22239057—

반응 조건

온도-10 °C

반응 단계

Dry, pulverulent lithium hydroxide (11.55 mmol, 3.3 equivalents) is added in one portion to a well-stirred solution of 2,4-dihydroxyacetophenone (3.22 mmol) in dry THF (5 ml) under an argon atmosphere at −78° C. The reaction mixture is stirred at −78° C. for one hour and subsequently at −10° C. for two hours. After the mixture has been re-cooled to −78° C., a solution of 9-fluorenone-4-carbonyl chloride (3.3 mmol) in THF (10 ml) is added in one portion. The mixture is stirred at −78° C. for one hour and at room temperature for 4 hours until the starting material has disappeared. The reaction mixture is emptied into a mixture of ice (150 g) and concentrated HCl (5 ml) and extracted with chloroform (3×50 ml). The solvents are removed from the dried extracts, and the residue is dried under reduced pressure for 24 hours. Glacial acetic acid (30 ml) and sulfuric acid (0.2 ml) are added to the residue, and the mixture is heated at 95–100° C. for from 30 minutes to one hour under an argon atmosphere. Approximately one third of the acetic acid is stripped off, and the residue is emptied into water. The precipitated product is filtered, washed and dried and recrystallised in methanol, giving 2-(9-fluorenon-4-yl)hydroxychromone. EI-MS (70 eV) m/e (rel. abund.)=340.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07009062B2
출처 데이터셋uspto-grants-2006_03
ORD IDord-b9219aab03b241509d7cd8cb7a69d0ef
출처 메모uspto-grants-2006_03