Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245562Generated: October 25, 2026

Benzene → Dibenzyl ethylmalonate

https://huagongshe.com/reaction/1245562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantBenzyl BromideHCID 7498—
ReactantEthylmalonic acidHCID 11756—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ProductDibenzyl ethylmalonateHCID 53752489—

Reaction Steps

A solution of 2.0 g (15 mmol) of ethyl-malonic acid, 4.7 mL (31 mmol) of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) and 3.9 mL (32 mmol) of benzyl bromide in 100 mL of benzene was refluxed for 22 hours. After cooling, the reaction was washed with 150 mL of H2O. After separating layers, the organic phase was dried over MgSO4 and concentrated. The residue was purified on a 40M Biotage column using 24:1 v/v hexane/EtOAc as the eluant to afford the title compound as a colorless oil: RF: 0.40 (9:1 v/v hexane/EtOAc); 1H-NMR (500 MHz) δ 0.97 (t, J=7.4, 3H), 1.99 (quint, J=7.4, 2H), 3.39 (t, J=7.4, 1H), 5.17 (s, 2H), 7.29–7.36 (m, 10H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125887B2
Source datasetuspto-grants-2006_10
ORD IDord-a9ef386b9fb540bf93afcf5cc3ee8541
Source noteuspto-grants-2006_10