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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750484Generated: October 31, 2026

Triethylamine → Methyl 3-ethenylpyridine-2-carboxylate

https://huagongshe.com/reaction/1750484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 3-bromo-2-pyridinecarboxylateHCID 12828946—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductMethyl 3-ethenylpyridine-2-carboxylateHCID 15257081—

Reaction Conditions

Temperature100 °C

Reaction Steps

Methyl 3-bromopyridine-2-carboxylate (1.0 g, 4.63 mmol) and potassium vinyltrifluoroborate (CAS number 13682-77-4; 0.744 g, 5.56 mmol) were dissolved in IPA (15 ml). To this was then added triethylamine (0.467 g, 4.63 mmol) and the mixture was degassed under nitrogen atmosphere for 15 minutes. [1,1′-Bis(diphenyl phosphino)ferrocene]dichloropalladium(II) (0.075 g, 0.092 mmol) was added and the reaction was stirred at 100° C. for 4 hours. The reaction was diluted with water (75 ml) and filtered through diatomaceous earth (commercially sold under the trade mark “Celite”). The organics were extracted with ethyl acetate (3×50 ml), washed with water (25 ml), brine (20 ml), dried over sodium sulfate and concentrated in vacuo. The resulting residue was purified by column chromatography (silica, 0-18% ethyl acetate/n-hexane to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156829B2
Source datasetuspto-grants-2015_10
ORD IDord-5f023345960c4a92b4a016f757b09621
Source noteuspto-grants-2015_10