HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176909Generated: October 30, 2026
4-Nitrobenzyl bromide → Diethyl 2-(4-nitrobenzyl)-2-methylmalonate
https://huagongshe.com/reaction/2176909
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 5088009 | HCID 5088009 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl 2-(4-nitrobenzyl)-2-methylmalonate | HCID 54496963 | 29.7% |
Reaction Steps
Diethyl methyl malonate (1.60 ml, 9.25 mmol) was added to a freshly prepared solution of sodium ethoxide solution [(sodium (212 mg, 9.25 mmol) in EtOH (20 ml)] and stirred for 1 h. 4-Nitrobenzyl bromide (2.00 g, 9.25 mmol) was added dropwise to the reaction mixture and stirred for 6 h at reflux. The reaction mixture was cooled to room temperature and concentrated. The residue was partitioned between water and CHCl3. The separated organic layer was washed with water, brine solution, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to give the crude product. This was purified by column chromatography over silica gel (100-200 mesh) using 5% ethyl acetate in petroleum ether as eluent to afford 850 mg (29.7%) of diethyl 2-(4-nitrobenzyl)-2-methylmalonate as oily liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067888B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-f8188fccd9b744dba58d28e814b8cad1 |
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| Source note | uspto-grants-2015_06 |
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