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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54972Generated: October 26, 2026

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

https://huagongshe.com/reaction/54972

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 numberUS05624922
Source datasetuspto-grants-1997_04
ORD IDord-0c4660183fbc41969b1652484277c365
Source noteuspto-grants-1997_04