HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537123Generated: October 26, 2026
Diethyl Malonate → Diethyl 2-(5-bromo-3-nitropyridin-2-yl)malonate
https://huagongshe.com/reaction/537123
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| 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 | 69.3% |
Reaction Steps
To a suspension of sodium hydride (5.08 g, 127 mmol) in N,N-dimethylformamide (75 mL) was added diethyl malonate (19.26 mL, 127 mmol) at 0° C. The solution was then stirred at ambient temperature for 30 minutes and a solution of 5-bromo-2-chloro-3-nitropyridine (30 g, 127 mmol) in N,N-dimethylformamide (75 mL) was added dropwise. The dark brown mixture was then stirred at 100° C. for 2 hours before being cooled to ambient temperature and quenched with a saturated solution of ammonium chloride (500 mL) at 0° C. The mixture was extracted with ethyl acetate (3×500 mL) and the combined organics were dried over magnesium sulfate and filtered. The solvent was removed in vacuo to give a dark brown oil which was purified by flash column chromatography (10% ethyl acetate/hexane) to afford diethyl 2-(5-bromo-3-nitropyridin-2-yl)malonate as a brown solid (31.8 g, 69%). 1HNMR (400 MHz, CDCl3, δ): 8.86 (s, 1H), 8.61 (s, 1H), 5.44 (s, 1H), 4.29 (q, 4H), 1.27 (t, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859773B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-4ae739488f1f4a389b9426437d92cb77 |
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| Source note | uspto-grants-2014_10 |
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