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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958627Generated: November 1, 2026

Potassium Carbonate → Pyridine, 2,6-dichloro-4-[1-(trifluoromethyl)ethenyl]-

https://huagongshe.com/reaction/1958627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(3,3,3-Trifluoroprop-1-en-2-yl)boronic acidHCID 2782677—
Reactant2,6-Dichloro-4-iodopyridineHCID 11737393—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductPyridine, 2,6-dichloro-4-[1-(trifluoromethyl)ethenyl]-HCID 8666462091.1%

Reaction Steps

2,6-dichloro-4-iodopyridine (0.87 g), (3,3,3-trifluoroprop-1-en-2-yl)boronic acid (purity: 65%, 0.75 g) and potassium carbonate (0.96 g) were dissolved in the mixed solvent of THF and water, which was then degassed three times. To the solution was added dichlorobis(triphenylphosphine) palladium (II) (0.04 g), and the mixture was heated to reflux for 3 hours under argon atmosphere. The mixture was cooled to room temperature and then poured into water, which was then extracted twice with hexane. The organic layer was combined, which was then washed with water and dried over anhydrous magnesium sulfate. After the drying agent was filtered off, the solvent was distilled away under reduced pressure, and the residue was then purified by silica gel chromatography to obtain 2,6-dichloro-4-(3,3,3-trifluoroprop-1-en-2-yl)pyridine (0.70 g) at a yield of 82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410141B2
Source datasetuspto-grants-2013_04
ORD IDord-9493ab656e414edcb2590b6e47b85908
Source noteuspto-grants-2013_04