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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300290Generated: November 1, 2026

Toluene → Ethyl 2-(3,4,5-trimethoxyphenyl)pyridine-4-carboxylate

https://huagongshe.com/reaction/2300290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant3,4,5-Trimethoxybenzeneboronic acidHCID 2734390—
ReactantEthyl 2-chloroisonicotinateHCID 2762942—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(3,4,5-trimethoxyphenyl)pyridine-4-carboxylateHCID 16125879—

Reaction Conditions

Temperature90 °C

Reaction Steps

3,4,5-Trimethoxyphenylboronic acid (20.10 g) and ethyl 2-chloroisonicotinate (18.56 g) were suspended in a mixted solvent of toluene (200 mL) and THF(100 mL), and to the suspension 2 M sodium carbonate (200 mL) and tetrakis(triphenyl phosphine) palladium(0) (5.78 g) were added. The mixture was stirred at 90° C. overnight under an argon atmosphere. Ethyl acetate was added to the reaction mixture to separate an organic layer. The organic layer was washed with brine, dried over anhydrous sodium magnesium and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using hexane-ethyl acetate (5:1) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498169B1
Source datasetuspto-grants-2002_12
ORD IDord-7e15c98146fe4ba599395979c813e6ff
Source noteuspto-grants-2002_12