HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114161Generated: October 30, 2026
Diethyl Malonate → Diethyl 2-(3-methyl-4-nitrophenyl)malonate
https://huagongshe.com/reaction/2114161
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% in mineral oil; 0.599 g) was suspended in dimethylformamide (10 mL), and to this was added dropwise a solution of diethyl malonate (2.00 g) in dimethylformamide (10 mL) under ice-cooling. After the foam generation was finished, a solution of 4-fluoro-2-methylnitrobenzene (1.94 g) in dimethylformamide (5 mL) was added thereto. The reaction temperature was raised to 100° C., the mixture was stirred for 6 hours. The resulting 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, concentrated, and purified by column chromatography on silica gel (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 | US07432392B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-16cac0b87fcf44fab50ead357fd552b7 |
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| Source note | uspto-grants-2008_10 |
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