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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665769Generated: October 30, 2026

Diethyl methylmalonate → Diethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonate

https://huagongshe.com/reaction/1665769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl methylmalonateHCID 11857—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-1-fluoro-4-nitrobenzeneHCID 69699—
SolventDimethylformamideHCID 6228—
ProductDiethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonateHCID 5920613299%

Reaction Conditions

Temperature0 °C

Reaction Steps

Diethyl 2-methylmalonate (4.31 mL, 25.0 mmol) was dissolved in 25 mL of anhydrous DMF. This solution was cooled to 0° C. under an atmosphere of nitrogen. Sodium hydride (1.04 g, 26 mmol, 60% by weight in mineral oil) was slowly added to the solution. The resulting mixture was allowed to stir for 3 minutes at 0° C., and then at room temperature for 10 minutes. 2-Bromo-1-fluoro-4-nitrobenzene (5.00 g, 22.7 mmol) was quickly added and the mixture turned bright red. After stirring for 10 minutes at room temperature, the crude mixture was evaporated to dryness and then partitioned between dichloromethane and a saturated aqueous solution of sodium chloride. The layers were separated and the organic phase was washed twice with a saturated aqueous solution of sodium chloride. The organics were concentrated to yield diethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonate (8.4 g, 99%) as a pale yellow oil which was used without further purification. Retention time 1.86 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039491B2
Source datasetuspto-grants-2011_10
ORD IDord-0dfa10188f174486b585cd780ae9f48c
Source noteuspto-grants-2011_10