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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241093Generated: November 3, 2026

Acetic Acid → 2,4'-Bipyridine

https://huagongshe.com/reaction/2241093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-AcetylpyridineHCID 14282—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium AcetateHCID 517165—
Reactant1,3-dimethyl-2,3-dihydro-2-oxopyrimidinium ChlorideHCID 23083342—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
Product2,4'-BipyridineHCID 6848880%

Reaction Steps

14.0 g (87 mmol) of 1,3-dimethyl-2,3-dihydro-2-oxopyrimidinium chloride obtained in Example 1 was dissolved in 25 ml of acetonitrile and mixed with 10 g (83 mmol) of 4-acetylpyridine, and 12.6 g (125 mmol) of triethylamine was added dropwise thereto at 45° C. or less. After 30 minutes of the reaction at 45° C., acetonitrile and triethylamine were evaporated under a reduced pressure, and 25 ml (416 mmol) of acetic acid and 39 g (454 mmol) of ammonium acetate were added to the residual liquid to carry out the reaction at 120° C. for 8 hours. After completion of the reaction, this was cooled to room temperature, neutralized with 217 g of 25% sodium hydroxide aqueous solution and then extracted three times with 200 ml of toluene. The organic layer was concentrated and then purified by distillation under a reduced pressure to obtain 10.3 g (yield 80%) of the title compound (purity 99.9%, melting point 56-57° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723522B2
Source datasetuspto-grants-2010_05
ORD IDord-efaf63fc123240fc83bf711e3f51a450
Source noteuspto-grants-2010_05