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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305098Generated: November 1, 2026

4-Vinylpyridine → HCID 54192486, compound

https://huagongshe.com/reaction/2305098

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-VinylpyridineHCID 7502—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22872668HCID 22872668—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 54192486HCID 5419248653%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-bromo-6-chloro-3-(1-BOC-2-(S)-pyrrolidinylmethoxy)pyridine (500 mg, 1.28 mmol) in acetonitrile (4.0 mL) was added 4-vinylpyridine (156 mg, 1.5 mmol), palladium acetate (29.0 mg, 0.12 mmol), tri-o-tolylphosphine (156 mg, 0.12 mmol) and triethylamine (3.2 mL). The reaction mixture was heated in a sealed tube at 100° C. overnight, then cooled to room temperature. Minimum amount of saturated sodium bicarbonate was added to free the amine hydrochloride salt, and the mixture was extracted with EtOAc, dried (MgSO4), and concentrated. The residue was chromatographed on a silica gel column, eluting with 4 to 50% Et2O in hexane) to give the title compound (282 mg). MS (CI/NH3) m/z 416 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437138B1
Source datasetuspto-grants-2002_08
ORD IDord-87158b4ddb844416ba2db2e316ebe866
Source noteuspto-grants-2002_08