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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507973Generated: November 3, 2026

3-Formylphenylboronic acid → HCID 23157556, compound

https://huagongshe.com/reaction/507973

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Formylphenylboronic acidHCID 2734356—
ReactantHCID 23157240HCID 23157240—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventSodium CarbonateHCID 10340—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 23157556HCID 2315755638.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-[(4-Bromo-3,5-dimethylphenyl)thio]ethyl ethyl ether (2.41 g, 8.33 mmol) and (3-formylphenyl)boronic acid (1.37 g, 9.16 mmol) were dissolved in a mixture of 2 M aqueous sodium carbonate solution (24 mL), ethanol (8 mL) and toluene (24 mL), the air was substituted with argon gas, and tetrakis(triphenylphosphine)palladium(0) (0.48 g, 0.42 mmol) was added. The reaction mixture was stirred under an argon atmosphere at 80° C. for 16 hr. After cooling the reaction mixture, saturated brine was added and the mixture was extracted with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-hexane/ethyl acetate=5/1) to give the title compound (1.00 g, yield 38%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786165B2
Source datasetuspto-grants-2010_08
ORD IDord-95ba8aa4a29340d2bf67df53044e853d
Source noteuspto-grants-2010_08