참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Lithium Hydroxide | HCID 3939 | — |
| 반응물 | 2',4'-Dihydroxyacetophenone | HCID 6990 | — |
| 반응물 | 9-Fluorenone-4-carbonyl chloride | HCID 610142 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(9-Fluorenon-4-yl)hydroxychromone | HCID 22239057 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07009062B2 |
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| 출처 데이터셋 | uspto-grants-2006_03 |
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| ORD ID | ord-b9219aab03b241509d7cd8cb7a69d0ef |
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| 출처 메모 | uspto-grants-2006_03 |
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