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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2228668Erstellt: 25. Oktober 2026

1-Benzoylnaphthalene → Naphthalen-2-yl(phenyl)methanol

https://huagongshe.com/reaction/2228668

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-BenzoylnaphthaleneHCID 69503—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
ProduktNaphthalen-2-yl(phenyl)methanolHCID 57077295,3%

Reaktionsschritte

To a solution of benzoylnaphthalene (5.00 g, 21.5 mmol) in methanol (30 mL) was added sodium borohydride (400 mg, 10.8 mmol) with ice-cooling and the mixture was stirred at room temperature for 30 minutes. This reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water, dried over MgSO4, and filtered and the filtrate was concentrated under reduced pressure to provide 4.80 g of (2-naphthyl)phenylmethanol. To a solution of this compound (4.80 g, 20.5 mmol) in diisopropyl ether (30 mL) was added phosphorus tribromide (3.70 g, 13.7 mmol) with ice-cooling and the mixture was stirred at room temperature for 1 hour. This reaction mixture was diluted with water and extracted with diisopropyl ether. The organic layer was washed with water and saturated aqueous sodium hydrogen carbonate solution, dried over MgSO4, and filtered. The filtrate was concentrated under reduced pressure and the solid residue was recrystallized from diisopropyl ether-hexane to provide 4.10 g of the title compound. Yield 64%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06417213B2
Quelldatensatzuspto-grants-2002_07
ORD IDord-f987dc155cef4f94bb6f52cfac98612a
Quellennotizuspto-grants-2002_07