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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1275418Erstellt: 26. Oktober 2026

Hydrochloric Acid → 1-Benzoylnaphthalene

https://huagongshe.com/reaction/1275418

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktIodineHCID 807—
EduktDiethyl EtherHCID 3283—
Edukt1-NaphthalenecarbonitrileHCID 6846—
EduktBromobenzeneHCID 7961—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelMagnesiumHCID 5462224—
Produkt1-BenzoylnaphthaleneHCID 6950329%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06160175
Quelldatensatzuspto-grants-2000_12
ORD IDord-449c62ea40fa4d84965ad289fcaef310
Quellennotizuspto-grants-2000_12