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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480613Generated: October 29, 2026

Potassium Carbonate → 2-(5-(Tert-butyl)-2-methoxyphenyl)-5-methylpyridine

https://huagongshe.com/reaction/1480613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-5-methylpyridineHCID 564216—
Reactant5-(tert-Butyl)-2-methoxybenzeneboronic acidHCID 14740579—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(5-(Tert-butyl)-2-methoxyphenyl)-5-methylpyridineHCID 8671857099%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-bromo-5-methylpyridine [purchased from TCI] (0.827 g, 4.81 mmol), (5-(tert-butyl)-2-methoxyphenyl)boronic acid [Intermediate 5] (1.2 g, 5.77 mmol) and potassium carbonate (0.997 g, 7.21 mmol) in dimethoxyethane (15 mL) and water (5 mL) was purged with nitrogen for 20 minutes. Tetrakis(triphenylphosphine)palladium(0) (277.8 mg, 0.24 mmol) was added and the reaction mixture heated to 80° C. in a sealed vial for 22 hours. The cooled reaction mixture was partitioned between ethyl acetate (80 mL) and 1 M aqueous sodium hydroxide solution (80 mL), the organic phase separated, washed with water (80 mL) and saturated brine (80 mL), dried (MgSO4), filtered and concentrated under reduced pressure to give a yellow syrup. The crude product was purified by chromatography on silica eluting with a solvent gradient of 0 to 35% ethyl acetate in hexanes to give 2-(5-(tert-butyl)-2-methoxyphenyl)-5-methylpyridine (1.216 g, 99% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409893B2
Source datasetuspto-grants-2016_08
ORD IDord-aac6ee9d5ff94983858b1920425c3d21
Source noteuspto-grants-2016_08