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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602116Generated: October 31, 2026

Hydrochloric Acid → Diethyl 2-(2,6-difluoro-4-methoxyphenyl)malonate

https://huagongshe.com/reaction/1602116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromo-3,5-difluoroanisoleHCID 2724984—
Catalystcopper(I) bromideHCID 24593—
Solvent1,4-DioxaneHCID 31275—
ProductDiethyl 2-(2,6-difluoro-4-methoxyphenyl)malonateHCID 1117413874.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

Diethyl malonate (0.505 mol) is added to a mixture of sodium hydride (0.412 mol) and 1,4-dioxane (230 ml) at 40° C. within 3 hours. The mixture is stirred for 90 minutes at 60° C. and copper(I) bromide (0.402 mol) is added. A mixture of 2,6-difluoro-4-methoxybromobenzene (0.2 mol) and 1,4-dioxane (50 ml) is added. The reaction mixture is heated at 100° C. for 14 hours and cooled to 15° C. Hydrochloric acid (12N, 350 ml) is added slowly at 15 to 20° C. The organic phase is separated off and the aqueous phase is extracted with ethyl acetate (250 ml) and toluene (200 ml). The combined organic phases are concentrated in vacuo. The residue is filtered over silica gel, washed with petroleum ether/ethyl acetate (15:1) and the solvent is distilled off. The residue is distilled in vacuo to yield 44.8 g of the product as an oil, 128-136° C. at 0.018 mbar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981534
Source datasetuspto-grants-1999_11
ORD IDord-8320b4f6287349889a26dc4438ed9b32
Source noteuspto-grants-1999_11