참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl vinyl ketone | HCID 6570 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Benzenamine, 3-chloro-, hydrochloride (1:1) | HCID 67336 | — |
| 촉매 | Zincchloride | HCID 3007855 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 7-Chloro-4-methylquinoline | HCID 170437 | — |
반응 단계
32.8 g. (0.2 mol) 3-chloroaniline hydrochloride, 81 g. ferric trichloride hexahydrate (0.3 mol), 3.0 g. redried anhydrous zinc chloride and 150 mL 95% ethanol were added into a 500 mL 3-neck flask equipped with a reflux condenser, a magnetic stirrer with heating, a thermometer and a constant-pressure dropping funnel, and the mixture was stirred and heated to 60° C. 12.6 g. (0.18 mol) methyl vinyl ketone was added slowly through the constant-pressure dropping funnel while maintaining the temperature at 60-70° C., followed by raising the temperature to reflux for 2 hours. After cooling, the mixed solution was added with 25% aqueous sodium hydroxide until alkaline. The solvent was then distilled off under reduced pressure until dry. The resulting solids were removed and repeatedly extracted with anhydrous ethyl ether. The extracts were collected, dried over anhydrous potassium carbonate and filtered. After removing the solvent, the residue was purified in a silica column using hexane/ethyl acetate (3:1) as the mobile phase to afford 11.38 g. of product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07709653B2 |
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| 출처 데이터셋 | uspto-grants-2010_05 |
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| ORD ID | ord-5ff7f23daf544bd983658a9dfac439fb |
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| 출처 메모 | uspto-grants-2010_05 |
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