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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61985Generated: October 28, 2026

Sodium Carbonate → HCID 68702253, compound

https://huagongshe.com/reaction/61985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-(Benzyloxy)-3-methoxybenzeneboronic acidHCID 10682603—
Reactant2-(3-Bromophenyl)-6-(trifluoromethyl)pyridineHCID 68699540—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 68702253HCID 68702253—

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-bromophenyl)-6-(trifluoromethyl)pyridine (1.063 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 as a clear oil, 1.072 g (70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09446012B2
Source datasetuspto-grants-2016_09
ORD IDord-0583d207b00a4355be42751cdf8c237d
Source noteuspto-grants-2016_09