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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401289Generated: October 30, 2026

Sodium Carbonate → HCID 67037289, compound

https://huagongshe.com/reaction/1401289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-(Benzyloxy)-3-methoxybenzeneboronic acidHCID 10682603—
Reactant2-(3-Bromophenyl)-1-oxo-6-(trifluoromethyl)-1lambda~5~-pyridineHCID 67037089—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 67037289HCID 67037289—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred solution of 4-benzyloxy-3-methoxyphenylboronic acid (1.0 g, 3.87 mmol) and 2-(3-bromo-phenyl)-6-trifluoromethyl-pyridine 1-oxide (1.12 g, 3.52 mmol) in toluene (10 mL) and ethanol (1 mL) at room temperature under argon was added 2 N aqueous sodium carbonate solution (5.41 mL, 10.82 mmol) followed by tetrakis(triphenylphosphine)palladium (0.22 g, 0.19 mmol). The resulting mixture was stirred at 90° C. for two hours and then allowed to cool to room temperature. The phases were separated and the aqueous phase was extracted with toluene (5 mL). The combined organic phases were washed with water and brine, then dried over anhydrous sodium sulphate and filtered. Evaporation of the solvent left a brown oil that was chromatographed over silica gel (petroleum ether/ethyl acetate, 9:1) to give 2-(4′-benzyloxy-3′-methoxybiphenyl-3-yl)-6-trifluoromethyl-pyridine 1-oxide as a clear oil, 1.11 g (70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907099B2
Source datasetuspto-grants-2014_12
ORD IDord-0a33e0a4b34f40c38830127feb3c34d4
Source noteuspto-grants-2014_12