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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474311Generated: October 30, 2026

Dichloromethane → 6-Ethenylpyridine-3-carbonitrile

https://huagongshe.com/reaction/1474311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant6-Bromopyridine-3-carbonitrileHCID 5005718—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product6-Ethenylpyridine-3-carbonitrileHCID 19045310—

Reaction Steps

To a stirring solution of 6-bromopyridine-3-carbonitrile (2.0 g, 10.9 mmol), in EtOH (70 mL) were added bis[(diphenylphosphino)ferrocene]dichloropalladium (II), complex with dichloromethane (0.892 mg, 0.10 mmol), potassium vinyl trifluoroborate (2.93 g, 21.9 mmol), triethylamine (3.0 mL, 21.9 mmol), and water (0.5 mL). The reaction mixture was heated to reflux. Upon completion as determined by reverse phase HPLC-MS (1-2 h) and TLC (eluent: 10% ethyl acetate in hexanes), the reaction was cooled to room temperature, and then was diluted with water and extracted with EtOAc. The combined organic layers were washed with brine and dried over MgSO4. The extracts were concentrated and chromatographed over a column of SiO2 (0-20% EtOAc/hexanes as eluent). Evaporation of the solvent yielded 6-ethenylpyridine-3-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018211B2
Source datasetuspto-grants-2015_04
ORD IDord-a608ca252bcb4605a4ee7cf62e4fb6e9
Source noteuspto-grants-2015_04