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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Bromo-2,3-dichloropyridine | HCID 12747760 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl 2-(5-bromo-3-chloropyridin-2-yl)malonate | HCID 67979448 | 52% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09248129B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-651e78b3c15742858f53e2f7edf168a0 |
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| Source note | uspto-grants-2016_02 |
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