HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463761Generated: November 2, 2026
Diethyl Malonate → Diethyl 2-[(4-nitrophenyl)methyl]propanedioate
https://huagongshe.com/reaction/1463761
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diethyl 2-[(4-nitrophenyl)methyl]propanedioate | HCID 348576 | — |
Reaction Steps
21.4 g of lithium diisopropyl amide was added to 210 ml anhydrous tetrahydrofuran in a stream of nitrogen in a dry 3-necked flask with a drying tube and dropping funnel with pressure compensation. Next, 58.0 g of malonic acid diethyl ester in 100 ml anhydrous tetrahydrofuran was added dropwise at room temperature in 40 minutes. After 30 minutes the reaction solution was cooled to -62° C. and 39.1 g of 4-nitrobenzyl bromide in tetrahydrofuran was slowly added dropwise with vigorous agitation, followed by agitation for a further hour at -62° C., after which the precipitate was filtered cold. The filtrate was concentrated in a rotary evaporator, and the residue was dissolved in 300 ml ethanol at 65° C. and separated from the insoluble residue. 34.7 g of faintly yellowish crystals were obtained after cooling.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05302370 |
|---|
| Source dataset | uspto-grants-1994_04 |
|---|
| ORD ID | ord-3da41bfd164b48d0bf8b0755d3624442 |
|---|
| Source note | uspto-grants-1994_04 |
|---|