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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672205Generated: October 30, 2026

Acetic Acid → Diethyl 2-(5-bromo-3-nitropyridin-2-yl)malonate

https://huagongshe.com/reaction/1672205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium hydrideHCID 24758—
ReactantPropanedioic acid, monoethyl esterHCID 3595298—
Reactant5-Bromo-2-chloro-3-nitropyridineHCID 7019412—
SolventDimethylformamideHCID 6228—
ProductDiethyl 2-(5-bromo-3-nitropyridin-2-yl)malonateHCID 5751627599%

Reaction Steps

To a suspension of NaH (60% in mineral oil, 27.9 g, 0.69 mol) in DMF (300 mL) at 5-10° C. was slowly added ethyl malonate (125 mL, 0.69 mol) over 30 min. The mixture was allowed to stir for 20 min at rt, during which time the suspension became a solution. A solution of 5-bromo-2-chloro-3-nitropyridine (75 g, 0.32 mol) in DMF (75 mL) was added slowly at 5-10° C. The resulting dark red mixture was allowed to stir at 40° C. for 2 h. The reaction mixture was then poured into 1M AcOH (0.75 L) and extracted with DCM (3×250 mL). The organic solutions were combined, washed with water and brine, dried over MgSO4, filtered and concentrated. The residue was purified by column chromatography to give diethyl(5-bromo-3-nitropyridin-2-yl)malonate (260 g, 99%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998952B2
Source datasetuspto-grants-2011_08
ORD IDord-f2065309539c4fa0b4a61a7bb746101e
Source noteuspto-grants-2011_08