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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071019Generated: October 26, 2026

Dichloromethane → 1-(5-(Prop-1-en-2-yl)pyridin-3-yl)ethanone

https://huagongshe.com/reaction/2071019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant3-Acetyl-5-bromopyridineHCID 820423—
ReactantPotassiumHCID 5462222—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventIsopropanolHCID 3776—
Product1-(5-(Prop-1-en-2-yl)pyridin-3-yl)ethanoneHCID 686706053,170.7%

Reaction Steps

A stirred solution of 1-(5-bromopyridin-3-yl)ethanone (600 mg, 3.0 mmol), potassium isopopenyltrifluoroborate (148 mg, 3.0 mmol), and Et3N (1.25 mL, 9.0 mmol) in iPrOH (20 mL) and H2O (10 mL) was degassed with argon for 10 min and then PdCl2 (dppf).CH2Cl2 (74 mg, 0.09 mmol) was added and the reaction mixture was heated to reflux for 5 h. The solution was cooled to room temperature and diluted with Ether and H2O. The layers were separated and the aqueous layer was extracted with Ether (2×50 mL). The combined organic layer was washed with brine, dried with Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography (30% EtOAc in hexanes) to provide 460 mg of 1-(5-(prop-1-en-2-yl)pyridin-3-yl)ethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-0328a30d6b6c44d598c9f8922879ffcd
Source noteuspto-grants-2012_10