Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290319Generated: October 25, 2026

Diethyl Malonate → Diethyl 2-(1-Bromo-2-naphthylmethyl)malonate

https://huagongshe.com/reaction/1290319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
Reactant1-Bromo-2-(bromomethyl)naphthaleneHCID 37828—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductDiethyl 2-(1-Bromo-2-naphthylmethyl)malonateHCID 1449149295.6%

Reaction Steps

To a solution of NaOEt prepared from 9.66 g of sodium and 210 mL of dry EtOH was added 63.76 mL of diethyl malonate and the reaction mixture refluxed for 2 h. To the resulting yellow solution was added in small portions 126 g of 1-bromo-2-bromomethylnaphthalene and the reaction mixture refluxed for 16 h. Distillation of ethanol from an oil bath (100°-110° C.) through a simple Claisen head gave a yellow suspension, to which was added 350 mL of CH2Cl2 and 350 mL of H2O. The aqueous layer was extracted twice with 120-mL portions of CH2Cl2, and the combined organic layer was washed three times with 100-mL portion of H2O, dried (MgSO4) and evaporated to give 152 g (95.6%) of the ester as a yellow solid, mp 60°-65° C. Recrystallization from acetic acid gave 137 g (86.2%) of the pure diester as a colorless solid, mp 77°-79° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750767
Source datasetuspto-grants-1998_05
ORD IDord-edce69a42435422ba59d585e8c0d274a
Source noteuspto-grants-1998_05