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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Propanedioic acid, monoethyl ester | HCID 3595298 | — |
| Reactant | 5-Bromo-2-chloro-3-nitropyridine | HCID 7019412 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl 2-(5-bromo-3-nitropyridin-2-yl)malonate | HCID 57516275 | 99% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998952B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-f2065309539c4fa0b4a61a7bb746101e |
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| Source note | uspto-grants-2011_08 |
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