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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl methylmalonateHCID 11857—
Reactant4-Bromobenzyl bromideHCID 68527—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductDiethyl 2-(4-bromobenzyl)-2-methylmalonateHCID 21186275—

Reaction Conditions

Temperature5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060475
Source datasetuspto-grants-2000_05
ORD IDord-2458c7c4d15f4651babe02a3166568b7
Source noteuspto-grants-2000_05