참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | Cumene | HCID 7406 | — |
| 반응물 | 5-Hydroxy-5-phenyl-5,6,7,8-tetrahydroquinaldine | HCID 13345752 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 생성물 | 2-Methyl-5-phenylquinoline | HCID 22450270 | — |
반응 단계
A mixture of 20 g (0.084 mole) of 5-hydroxy-5-phenyl-5,6,7,8-tetrahydroquinaldine, 10 g of 10% palladium on carbon, 2.3 g of para-toluenesulfonic acid and 200 ml of cumene was heated at its reflux temperature for 24 hours. The mixture was filtered hot, and then the filtrate was evaporated to provide a residue. This residue was dissolved in dilute hydrochloric acid. This solution was extracted with diethyl ether and the acid layer was then neutralized with 50% aqueous sodium hydroxide solution. The product was extracted into diethyl ether. The organic layer was dried and then evaporated to provide a solid residue. Recrystallization from methanol provided white crystals of 5-phenylquinaldine. Analysis: Calculated for C16H13N.H2O: %C, 81.0; %H, 6.4; %N, 5.8; Found: %C, 81.4; %H, 6.6; %N, 5.5. The structure assignment was confirmed by nuclear magnetic resonance spectral analysis.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04603199 |
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| 출처 데이터셋 | uspto-grants-1986_07 |
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| ORD ID | ord-0fc275a1059540eb85407cb2dba41af9 |
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| 출처 메모 | uspto-grants-1986_07 |
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