HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzyl chloride → Diethyl benzyl-4-nitrobenzylmalonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzyl chloride | HCID 7482 | — |
| Reactant | Diethyl 2-benzylpropanedioate | HCID 69090 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl benzyl-4-nitrobenzylmalonate | HCID 53932722 | 71.2% |
Reaction Steps
To a stirred solution of p-nitrobenzyl chloride (15 g) and diethyl benzylmalonate (22 g) in N,N-dimethylformamide (150 ml) was added Nail (60% in oil, 3.8 g). After stirring at room temperature for 2 days, the reaction mixture was concentrated under reduced pressure and the residue was suspended in ethyl acetate. The ethyl acetate layer was washed with aqueous citric acid solution, water, saturated aqueous sodium hydrogen carbonate solution and brine, and dried (MgSO4). The organic solvent was evaporated off and the residual oil was purified by column chromatography on silica gel. Elution with ethyl acetate-hexane (1:6, v/v) gave diethyl benzyl-4-nitrobenzylmalonate (24 g, 71%) as crystals. Melting point: 70°-71° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05498728 |
| Source dataset | uspto-grants-1996_03 |
| ORD ID | ord-4cf3741791434fbe88f2d4c6c6df3b11 |
| Source note | uspto-grants-1996_03 |