HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174314Generated: November 2, 2026
Diethyl Malonate → Diethyl 2-[(4-nitrophenyl)methyl]propanedioate
https://huagongshe.com/reaction/2174314
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Diethyl 2-[(4-nitrophenyl)methyl]propanedioate | HCID 348576 | 88% |
Reaction Steps
4-Nitrobenzyl bromide 22 (10.57 g, 48.93 mmol) was added to a solution of diethyl malonate 21 (52 mL, 54.86 g, 342.51 mmol) and K2CO3 (14.21 g, 102.8 mmol) in acetone (40 mL). The reaction mixture was heated at 45° C. for 1 hour. The mixture was allowed to cool to room temperature and the resulting yellow slurry was filtered off to remove K2CO3 and washed with acetone (2×20 mL). The solvent was evaporated from the combined filtrate and washings under reduced pressure. The excess of diethylmalonate was removed by horizontal distillation (2 hr, 80-130° C., and 0.005 mbar). The yellow oily residue was dissolved in ethanol (200 mL). The precipitated white solid (dialkylated product) was filtered and washed with ethanol (2×20 mL). The solvent was evaporated from the combined filtrate and washings under reduced pressure to give a solid, which was recrystallized from hexane/Et2O (1:1) to afford white crystalline needles 23 (12.72 g, 88% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09061078B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-5dffa42eb0d0474693a71003351c54a4 |
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| Source note | uspto-grants-2015_06 |
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