HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494383Generated: October 30, 2026
Diethyl Malonate → Diethyl 2-(3-methyl-4-nitrophenyl)malonate
https://huagongshe.com/reaction/494383
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Fluoro-2-nitrotoluene | HCID 94956 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl 2-(3-methyl-4-nitrophenyl)malonate | HCID 23130308 | 44.7% |
Reaction Steps
Sodium hydride (60% mineral oil; 0.599 g) was suspended in dimethylformamide (10 mL), and a solution of malonic acid diethyl ester (2.00 g) in dimethylformamide (10 mL) was added dropwise thereto under ice-cooling. After foam generation is stopped, a solution of 4-fluoro-2-methylnitrobenzene (1.94 g) in dimethylformamide (5 mL) was added thereto, and the reaction temperature was raised to 100° C., followed by stirring for 6 hours. The reaction mixture was concentrated, acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was washed successively with water and saturated brine, dried over sodium sulfate and concentrated. The residue was purified by column chromatography on silica gel with ethyl acetate:hexane=1:5 to give the title compound (1.65 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538140B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-23cb197cf3ae444bb2d9f7b7d2a4988c |
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| Source note | uspto-grants-2009_05 |
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