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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Vinylpyridine | HCID 14272 | — |
| Reactant | 4-Iodo-2-phenylbenzoic acid methyl ester | HCID 53689979 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 4-[2-(3-Pyridyl)ethenyl]-2-phenylbenzoic Acid Methyl Ester | HCID 69892616 | 84.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06693123B2 |
|---|
| Source dataset | uspto-grants-2004_02 |
|---|
| ORD ID | ord-83f91f8c70494eae9e6968ad95c5bbbc |
|---|
| Source note | uspto-grants-2004_02 |
|---|