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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601141Generated: October 31, 2026

Dimethylformamide → Diethyl (3-nitropyridin-2-yl)propanedioate

https://huagongshe.com/reaction/1601141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-3-nitropyridineHCID 79613—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductDiethyl (3-nitropyridin-2-yl)propanedioateHCID 13147345—

Reaction Conditions

Temperature25 °C

Reaction Steps

50 g (0.31 mol) of diethyl malonate were added, a little at a time, at not more than 50° C. to a mixture of 7.5 g (0.31 mol) of sodium hydride and 50 ml of dimethylformamide, with ice-cooling. After the mixture had cooled to room temperature (approximately 25° C.), it was treated with g (0.173 mol) of 2-chloro-3-nitropyridine. After approximately 15 hours, the reaction mixture was diluted with water, acidified using acetic acid and extracted using ethyl acetate. The organic phases were combined, washed and dried, and the solvent was removed under reduced pressure. The excess malonic ester was distilled off at elevated temperature and reduced pressure ("high vacuum"). This gave 43 g (66%) of the title compound as a yellow oil (purity approximately 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977146
Source datasetuspto-grants-1999_11
ORD IDord-4857b5f1e46445c2aa7e20ef98033d55
Source noteuspto-grants-1999_11