Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348542Generated: October 26, 2026

Hydrochloric Acid → Propanedioic acid, 2-(2,4,6-trifluorophenyl)-, 1,3-diethyl ester

https://huagongshe.com/reaction/1348542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
Reactant1-Bromo-2,4,6-trifluorobenzeneHCID 75398—
SolventWaterHCID 962—
Solventtert-Butyl methyl etherHCID 15413—
Solvent1,4-DioxaneHCID 31275—
ProductPropanedioic acid, 2-(2,4,6-trifluorophenyl)-, 1,3-diethyl esterHCID 278266243.4%

Reaction Conditions

Temperature40 °C

Reaction Steps

Into a mixture of 4.8 g of sodium hydride (60% in oil) and 100 ml of 1,4-dioxane, 19.2 g of diethyl malonate were added dropwise at room temperature, and then 17.2 g of cuprous bromide and 21.1 g of 1-bromo-2,4,6-trifluorobenzene were subsequently added thereto at 40° C. and refluxed for 26 hours under heating. To the reaction mixture, conc. hydrochloric acid was added under ice-cooling, and then tert-butyl methyl ether and water were added. The organic layer was separated, washed with aqueous sodium hydroxide solution, dil. hydrochloric acid and water subsequently, dried over sodium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give 12.6 g of diethyl (2,4,6-trifluorophenyl)malonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211545B2
Source datasetuspto-grants-2007_05
ORD IDord-ddc6f29da12c4e8aacd3f30c97566c76
Source noteuspto-grants-2007_05