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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507905Generated: October 27, 2026

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

https://huagongshe.com/reaction/507905

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-dimethylphenylboronic acid (21.0 g, 140 mmol) were dissolved in a mixture of 1 M aqueous sodium carbonate solution (200 mL), ethanol (100 mL) and toluene (200 mL). The air was substituted with argon gas, and 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. After cooling the reaction mixture, water was added and the mixture was diluted with ethyl acetate. The insoluble material was filtered off through celite. The organic layer in 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 numberUS07786165B2
Source datasetuspto-grants-2010_08
ORD IDord-2054364760e3496b99f1f74761d5805d
Source noteuspto-grants-2010_08