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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770898Generated: October 26, 2026

Diethyl Malonate → Diethyl 2-(5-bromo-3-chloropyridin-2-yl)malonate

https://huagongshe.com/reaction/1770898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-2,3-dichloropyridineHCID 12747760—
SolventDimethylformamideHCID 6228—
ProductDiethyl 2-(5-bromo-3-chloropyridin-2-yl)malonateHCID 6797944852%

Reaction Steps

Diethyl malonate (0.87 mL, 5.7 mmol) was added dropwise to a suspension of NaH (55% in mineral oil, 0.27 g, 6.2 mmol) in DMF (6 mL) at 0° C. The ice-bath was removed and the mixture was stirred under N2 at r.t. for 20 min. 5-Bromo-2,3-dichloropyridine (1.0 g, 4.4 mmol) was added, and the mixture was stirred at 120° C. overnight. The mixture was allowed to cool and was then partitioned between water containing NaCl and EtOAc. The organic phase was dried (MgSO4) and evaporated to give a crude product which was purified by flash chromatography (25 g SiO2, heptane/EtOAc gradient) affording the title compound (0.8 g, 2 mmol, 52% yield) containing a residue of unreacted malonic ester. MS (ES+) m/z 350 [M+H]+. A part of this material was used as such in the subsequent step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248129B2
Source datasetuspto-grants-2016_02
ORD IDord-651e78b3c15742858f53e2f7edf168a0
Source noteuspto-grants-2016_02