참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Tropolone | HCID 10789 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Dicyclohexano-18-crown-6 | HCID 85955 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 2-Methoxy-2,4,6-cycloheptatrien-1-one | HCID 16546 | 92% |
반응 단계
To the mixture of 20 g (0.16 mol) of tropolone (2-hydroxy-2,4,6-cycloheptatrienone), 68 g (0.48 mol) of anhydrous potassium carbonate, 6.1 g (0.016 mol) of dicyclohexyl-18-crown-6 and 750 ml of acetonitrile were added 117 g (0.8 mol) of methyl iodide with stirring. After stirred under reflux for 10 hours, the reaction mixture was filtered. The filtrate was concentrated under reduced pressure, and the residue was dissolved in dichloromethane. After washing with 13.8% aqueous solution of potassium carbonate and water. After drying with magnesium sulfate anhydrous, dichloromethane was evaporated under reduced pressure, and the residue was subjected to purification by means of silica gel column chromatography. Elution was carried out by using ethyl acetate and the solvent was evaporated under reduced pressure to give 20 g of 2-methoxytropone (2-methoxy-2,4,6-cycloheptatrienone) (yield: 92%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | USRE034918 |
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| 출처 데이터셋 | uspto-grants-1995_04 |
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| ORD ID | ord-920935019f514e81b570eee36a1e4e16 |
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| 출처 메모 | uspto-grants-1995_04 |
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