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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15052Generated: October 26, 2026

Ethanol → 5-Chloro-2-ethenylpyridine

https://huagongshe.com/reaction/15052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
Reactant2,5-DichloropyridineHCID 27685—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
CatalystHCID 178478230HCID 178478230—
SolventEthyl AcetateHCID 8857—
Product5-Chloro-2-ethenylpyridineHCID 1554762669%

Reaction Steps

A mixture of 2,5-dichloropyridine (10.0 g), potassium vinyltrifluoroborate (10.86 g), dichloromethane complex (2.5 g) of dichloro-1,1′-bis(diphenylphosphino)-ferrocene palladium (II), triethylamine (14.13 mL) and ethanol (150 mL) was stirred overnight under reflux. After cooling the system to room temperature, ethyl acetate was added, followed by washing with saturated aqueous sodium hydrogencarbonate solution and saturated brine and drying over anhydrous sodium sulfate. Concentrating the solvent under reduced pressure, the resulting residue was distilled under reduced pressure (63° C., 8 mmHg) to provide the title compound (6.50 g, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732456B2
Source datasetuspto-grants-2010_06
ORD IDord-9ed94748395b45b697f76c4f2d4a5178
Source noteuspto-grants-2010_06