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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303347Generated: October 31, 2026

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

https://huagongshe.com/reaction/2303347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant3,4,5-Trimethoxybenzeneboronic acidHCID 2734390—
ReactantEthyl 2-chloroisonicotinateHCID 2762942—
CatalystHCID 178418397HCID 178418397—
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 (20.64 g) and ethyl 2-chloroisonicotinate (19.06 g) were suspended in a mixed solvent of toluene (200 mL) and THF (100 mL), and to the suspension 2 M sodium carbonate (200 mL) and tetrakis(triphenylphosphine)palladium(0) (5.93 g) were added. The mixture was stirred overnight at 90° C. under an argon atmosphere. Ethyl acetate was added to the reaction mixture to separate an organic layer. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=5:1) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432957B1
Source datasetuspto-grants-2002_08
ORD IDord-458de1f71d6f4923a57d9b1637eda67c
Source noteuspto-grants-2002_08