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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3,4,5-Trimethoxybenzeneboronic acid | HCID 2734390 | — |
| Reactant | Ethyl 2-chloroisonicotinate | HCID 2762942 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-(3,4,5-trimethoxyphenyl)pyridine-4-carboxylate | HCID 16125879 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06432957B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-458de1f71d6f4923a57d9b1637eda67c |
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| Source note | uspto-grants-2002_08 |
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