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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121225Generated: November 3, 2026

Dichloromethane → 4-[2-(3-Pyridyl)ethenyl]-2-phenylbenzoic Acid Methyl Ester

https://huagongshe.com/reaction/2121225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant3-VinylpyridineHCID 14272—
Reactant4-Iodo-2-phenylbenzoic acid methyl esterHCID 53689979—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-[2-(3-Pyridyl)ethenyl]-2-phenylbenzoic Acid Methyl EsterHCID 6989261684.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of the 4-iodo-2-phenylbenzoic acid methyl ester (6.11 g, 18.1 mmol), prepared as in Example 210C, 3-vinylpyridine (2.85 g, 27.1 mmol), prepared as in Example 210E, [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) chloride, complexed to dichloromethane (1:1) (444 mg, 0.543 mmol) and triethylamine (5.05 g, 36.2 mmol), in 1-methyl-2-pyrrolidinone (30 mL) was degassed with nitrogen and heated at 80° C. for 18 hours. The reaction mixture was diluted with ether, filtered through silica gel, and rinsed with ethyl acetate. The filtrate was washed with water and brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography (30% ethyl acetate-hexane) to give the title compound (4.82 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693123B2
Source datasetuspto-grants-2004_02
ORD IDord-83f91f8c70494eae9e6968ad95c5bbbc
Source noteuspto-grants-2004_02