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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592130Generated: October 25, 2026

Toluene → Ethyl 2-(4-(2-methylpyridin-4-yl)phenyl)acetate

https://huagongshe.com/reaction/592130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
ReactantEthyl (4-iodophenyl)acetateHCID 14974990—
Reactant2-Methylpyridine-4-boronic acid pinacol esterHCID 16414274—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
ProductEthyl 2-(4-(2-methylpyridin-4-yl)phenyl)acetateHCID 58447956—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a sealed tube were added 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (2.2 g, 10 mmol), ethyl 2-(4-iodophenyl)acetate 26-1 (2.9 g, 10 mmol), Pd(PPh3)4 (0.231 g, 0.2 mmol), toluene (30 mL), ethanol (10 mL) and 2M Na2CO3 (10 mL). The reaction mixture was flushed with nitrogen and stirred at 90° C. for 10 hours. After cooled down to room temperature, the reaction mixture was diluted into 200 mL ethyl acetate and washed with saturated sodium bicarbonate solution and then brine. The organic phase was dried over Na2SO4 and then taken to dryness by rotary evaporation. The crude product was purified by silica gel flash chromatography, eluted with 50% ethyl acetate in hexane to give ethyl 2-(4-(2-methylpyridin-4-yl)phenyl)acetate 26-2 as an oil. MS m/z 256.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238646B2
Source datasetuspto-grants-2016_01
ORD IDord-12ecdbc9d793437094f0f3e0fb79a32f
Source noteuspto-grants-2016_01