HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107474Generated: October 30, 2026
Diethyl methylmalonate → Diethyl 2-(4-bromobenzyl)-2-methylmalonate
https://huagongshe.com/reaction/1107474
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl methylmalonate | HCID 11857 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl 2-(4-bromobenzyl)-2-methylmalonate | HCID 21186275 | — |
Reaction Steps
Sodium ethoxide was generated by the addition of sodium (9.45 g) to ethanol (370 ml). The resulting solution was cooled to 5° C. and diethyl 2-methylmalonate (68.8 ml) added over 2 minutes. The reaction mixture was stirred at 5° C. for 20 minutes and then 4-bromobenzyl bromide (97.0 g) was added over 20 minutes. The reaction mixture was then heated under reflux for 16 hours. The reaction mixture was cooled to ambient temperature, filtered through diatomaceous earth and evaporated. The residue was partitioned between water (500 mi) and diethyl ether (1000 ml). The diethyl ether was separated and the aqueous layer was extracted with diethyl ether (2×50oml). The combined organic layers were dried (MgSO4) and evaporated to give an amber oil. This was purified by vacuum distillation, affording diethyl 2-(4-bromobenzyl)-2-methylmalonate (84.4 g), b.p.122-125° C./0.1-0.2 mm Hg; mass spectrum (+ve CI): 343 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06060475 |
|---|
| Source dataset | uspto-grants-2000_05 |
|---|
| ORD ID | ord-2458c7c4d15f4651babe02a3166568b7 |
|---|
| Source note | uspto-grants-2000_05 |
|---|