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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769117Generated: October 27, 2026

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

https://huagongshe.com/reaction/1769117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant1-Bromo-2-methylnaphthaleneHCID 75754—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product(2-Methyl-1-naphthyl)(phenyl)methanolHCID 1995712078.7%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380721
Source datasetuspto-grants-1995_01
ORD IDord-eba79c607d4d46d8939b185d958588d9
Source noteuspto-grants-1995_01