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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581553Generated: October 26, 2026

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

https://huagongshe.com/reaction/1581553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
Reactant1-Bromo-2,4,6-trifluorobenzeneHCID 75398—
Catalystcopper(I) bromideHCID 24593—
Solvent1,4-DioxaneHCID 31275—
ProductPropanedioic acid, 2-(2,4,6-trifluorophenyl)-, 1,3-diethyl esterHCID 2782662—

Reaction Conditions

Temperature55 °C

Reaction Steps

Diethyl malonate (0.49 mol) was added to a mixture of sodium hydride (0.51 mol) and 1,4-dioxane (140 ml) at 55 to 60° C. within 2 hours. A mixture of 1,4-dioxane (50 ml) and diethyl malonate (0.13 mol) was added. The mixture was stirred for 10 minutes at 55° C. and copper(I) bromide (0.05 mol) was added. After 15 min. a mixture of 2-bromo-1,3,5-trifluorobenzene (0.25 mol) and 1,4-dioxane (10 ml) was added. The reaction mixture was heated at 100° C. for 15 hours and cooled to 15° C. Hydrochloric acid (12N, 35 ml) was added slowly at 15 to 20° C. The precipitate was filtered off. The filtrate was extracted with diethylether. The organic Phase was separated, dried with anhydrous sodium sulphate and filtered. The filtrate was evaporated under reduced Pressure to yield the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730680B2
Source datasetuspto-grants-2004_05
ORD IDord-a81ef9b6ed624d92a97063a28b6fea60
Source noteuspto-grants-2004_05