참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Iodine | HCID 807 | — |
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | 1-Naphthalenecarbonitrile | HCID 6846 | — |
| 반응물 | Bromobenzene | HCID 7961 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Magnesium | HCID 5462224 | — |
| 생성물 | 1-Benzoylnaphthalene | HCID 69503 | 29% |
반응 단계
To 10.3 g (65 mMol) of bromobenzene in 50 mL of diethyl ether, magnesium turnings were added. The reaction was initiated by adding a few crystals of iodine to about 5 mL of the bromobenzene solution, and warming gently. The remainder of the bromobenzene was then added at such a rate as to maintain a mild reflux. When the reaction had abated, 1-naphthonitrile was added slowly in 50 mL of diethyl ether. The mixture was allowed to stir at room temperature overnight. Water was added, and the mixture acidified to pH 1 with concentrated hydrochloric acid. Methylene chloride was added and the mixture was heated under reflux overnight. The layers were separated, and the organic layer was washed with brine and dried over magnesium sulfate. The subtitled product was crystallized from methylene chloride/hexane, then further purified by medium pressure column chromatography on silica gel, eluting with ethyl acetate:hexane/5:95. The desired product was obtained as a white crystalline solid (4.38 g; 29% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06160175 |
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| 출처 데이터셋 | uspto-grants-2000_12 |
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| ORD ID | ord-449c62ea40fa4d84965ad289fcaef310 |
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| 출처 메모 | uspto-grants-2000_12 |
|---|