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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748431Generated: October 29, 2026

Dimethylformamide → N,N-dimethyl-2-(2-methyl-4-pyridyl)ethenamine

https://huagongshe.com/reaction/748431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2,4-DimethylpyridineHCID 7936—
ReactantDiethylamineHCID 8021—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductN,N-dimethyl-2-(2-methyl-4-pyridyl)ethenamineHCID 71437809100.5%

Reaction Steps

n-Butyl lithium in hexane (1.6 M, 35 ml, 56 mmol) was added dropwise to a solution of 2,4-lutidine (5.0 g, 46 mmol) in tetrahydrofuran (50 ml) at −78° C., and the mixture was stirred at the same temperature for 30 minutes. Successively, diethylamine (5.1 g, 69 mmol) was added to the mixture, and the mixture was stirred at −78° C., and the mixture was stirred at the same temperature for 30 minutes. Furthermore, DMF (6.8 g, 93 mmol) was added to the mixture at −78° C., and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was combined with aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated to give the titled compound (7.5 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399759B2
Source datasetuspto-grants-2008_07
ORD IDord-43f08e36fe48443aaf858854f0825a66
Source noteuspto-grants-2008_07