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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422256Generated: October 31, 2026

1-Bromo-2-methylnaphthalene → 3-(2-Methylnaphthalen-1-yl)benzaldehyde

https://huagongshe.com/reaction/2422256

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-methylnaphthaleneHCID 75754—
Reactant3-Formylphenylboronic acidHCID 2734356—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
Product3-(2-Methylnaphthalen-1-yl)benzaldehydeHCID 2308303165%

Reaction Conditions

Temperature80 °C

Reaction Steps

1-Bromo-2-methylnaphthalene (3.32 g, 15.0 mmol) and (3-formylphenyl)boronic acid (2.13 g, 15.0 mmol) was dissolved in a mixture of 1 M sodium carbonate aqueous solution (30 mL), ethanol (15 mL) and toluene (30 mL) and, after argon substitution, tetrakis(triphenylphosphine)palladium (0) (0.867 g, 0.750 mmol) was added. The reaction mixture was stirred under an argon atmosphere at 80° C. for 24 hrs. The reaction mixture was cooled, diluted with water and ethyl acetate, and the insoluble material was filtered through celite. The organic layer of the filtrate was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-20% ethyl acetate/hexane) to give the title compound (2.39 g, yield 65%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960369B2
Source datasetuspto-grants-2011_06
ORD IDord-052080beb3114ebfaa9997b2d51d07d0
Source noteuspto-grants-2011_06