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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578954Generated: October 27, 2026

Dimethyl malonate → HCID 117600964, compound

https://huagongshe.com/reaction/578954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl malonateHCID 7943—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium BicarbonateHCID 516893—
Reactant4-Bromo-2-fluoro-5-methylbenzonitrileHCID 34175419—
CatalystTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
SolventEthyl AcetateHCID 8857—
ProductHCID 117600964HCID 11760096443.1%

Reaction Conditions

Temperature170 °C

Reaction Steps

Combined 4-bromo-2-fluoro-5-methylbenzonitrile (4 g, 18.69 mmol) and dimethyl malonate (29.9 mL, 262 mmol). While purging the mixture with nitrogen, added potassium carbonate (3.87 g, 28.0 mmol), potassium hydrogencarbonate (2.81 g, 28.0 mmol), tri-tert-butylphosphonium tetrafluoroborate (0.119 g, 0.411 mmol), and bis(dibenzylidineacetone)palladium (0) (0.118 g, 0.206 mmol). The reaction mixture was heated in an oil bath at 170° C. for 3 hours, then cooled, diluted with ethyl acetate, and filtered through Celite®. The filtrate was concentrated and the residue dissolved in EtOAc, extracted with 1M aqueous sodium hydroxide (2×), twice with 10% aqueous sodium chloride, and brine. The organic phase was dried over sodium sulfate, filtered, and concentrated in vacuo, then purified by flash chromatography to give the title compound (1.67 g, 43%) as a clear colorless oil. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 2.30 (s, 3 H) 3.67 (s, 2 H) 3.72 (s, 3 H) 7.10 (d, J=9.60 Hz, 1 H) 7.42 (d, J=6.32 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040522B2
Source datasetuspto-grants-2015_05
ORD IDord-de71ac59248c4d1a9e9d4f006d63121a
Source noteuspto-grants-2015_05