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HRID 1275418作成日:2026年10月27日

Hydrochloric Acid → 1-Benzoylnaphthalene

https://huagongshe.com/reaction/1275418

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物IodineHCID 807—
反応物Diethyl EtherHCID 3283—
反応物1-NaphthalenecarbonitrileHCID 6846—
反応物BromobenzeneHCID 7961—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒MagnesiumHCID 5462224—
生成物1-BenzoylnaphthaleneHCID 6950329%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06160175
出典データセットuspto-grants-2000_12
ORD IDord-449c62ea40fa4d84965ad289fcaef310
出典メモuspto-grants-2000_12