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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1275418생성일: 2026년 10월 27일

Hydrochloric Acid → 1-Benzoylnaphthalene

https://huagongshe.com/reaction/1275418

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IodineHCID 807—
반응물Diethyl EtherHCID 3283—
반응물1-NaphthalenecarbonitrileHCID 6846—
반응물BromobenzeneHCID 7961—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매MagnesiumHCID 5462224—
생성물1-BenzoylnaphthaleneHCID 6950329%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06160175
출처 데이터셋uspto-grants-2000_12
ORD IDord-449c62ea40fa4d84965ad289fcaef310
출처 메모uspto-grants-2000_12