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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866086Generated: November 2, 2026

Hydrochloric Acid → Dimethyl(2-chloro-4-cyanophenyl)malonate

https://huagongshe.com/reaction/1866086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromo-3-chlorobenzonitrileHCID 16659395—
Catalystcopper(I) bromideHCID 24593—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductDimethyl(2-chloro-4-cyanophenyl)malonateHCID 5797744294.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

7.6 g (0.191 mol) of 60% strength sodium hydride in paraffin oil were initially charged in 300 ml of dioxane. At from 55° C. to 60° C., 22.9 g (0.173 mol) of diethyl malonate were added dropwise, and the mixture was stirred at 50° C. for 1-2 hours. 9.9-g (0.069 mol) of copper(1) bromide were added. At 80° C., 15 g (0.069 mol) of 3-chloro-4-bromobenzonitrile were then added dropwise, and the mixture was subsequently stirred at 100° C. for 14 hours. The reaction mixture was then cooled and acidified by dropwise addition of concentrated hydrochloric acid at from 15° C. to 20° C. Water was added, the mixture was extracted with dichloromethane, the organic phase was dried over sodium sulphate and the solvent was removed. The residue was distilled at 1 mbar, giving 17.5 g of dimethyl(2-chloro-4-cyanophenyl)malonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629294B2
Source datasetuspto-grants-2009_12
ORD IDord-eb4ad380124f472fbedda80532c3e92a
Source noteuspto-grants-2009_12