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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54972Erstellt: 23. Oktober 2026

Benzaldehyde → (2-Methyl-1-naphthyl)(phenyl)methanol

https://huagongshe.com/de/reaction/54972

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
Edukt1-Bromo-2-methylnaphthaleneHCID 75754—
EduktMagnesiumHCID 5462224—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(2-Methyl-1-naphthyl)(phenyl)methanolHCID 1995712078,7%

Reaktionsschritte

A solution of 10 g (45 mmol) of 1-bromo-2-methylnaphthalene in 75 mL of THF was refluxed with 1.2 g (50 mmol) of magnesium turnings for three hours. The reaction was cooled on ice and 4.8 mL (43 mmol) of benzaldehyde was added. The ice was removed, the reaction was stirred 45 minutes and quenched with 5 mL of 1N HCl followed by 50 mL of water. The reaction was extracted into ethyl acetate, dried over sodium sulfate and flash chromatographed through silica gel with 5-10% ethyl acetate in hexane to provide 8.4 g (75%) of 2-methyl-a-phenyl-1-naphthalenemethanol as a pale yellow gum.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05624922
Quelldatensatzuspto-grants-1997_04
ORD IDord-0c4660183fbc41969b1652484277c365
Quellennotizuspto-grants-1997_04