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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163282Generated: November 1, 2026

Water → 2',6'-Dimethylbiphenyl-3-carbaldehyde

https://huagongshe.com/reaction/1163282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-BromobenzaldehydeHCID 76583—
Reactant2,6-Dimethylphenylboronic acidHCID 583322—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
Product2',6'-Dimethylbiphenyl-3-carbaldehydeHCID 2308286697%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Bromobenzaldehyde (18.5 g, 100 mmol) and (2,6-dimethylphenyl)boronic acid (21.0 g, 140 mmol) were dissolved in a mixed solvent of 1 M aqueous sodium carbonate solution (200 mL), ethanol (100 mL) and toluene (200 mL). After argon substitution, tetrakis(triphenylphosphine)palladium(0) (5.78 g, 5.00 mmol) was added. The reaction mixture was stirred under an argon atmosphere at 80° C. for 20 hr. The reaction mixture was cooled, and water was added to the reaction mixture. The mixture was diluted with 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-10% ethyl acetate/hexane) to give the title compound (20.4 g, yield 97%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820837B2
Source datasetuspto-grants-2010_10
ORD IDord-07736b8a08144f1eb2b21fdbdd355f34
Source noteuspto-grants-2010_10