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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054721Generated: October 27, 2026

Picolinic acid → Diethyl 2-(4-bromo-2-methoxyphenyl)malonate

https://huagongshe.com/reaction/1054721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolinic acidHCID 1018—
ReactantCesium carbonateHCID 10796—
Reactant1,4-DioxaneHCID 31275—
Reactant2,2-DiethylpropanedioateHCID 6951563—
Reactant4-Bromo-1-iodo-2-methoxybenzeneHCID 46835731—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
ProductDiethyl 2-(4-bromo-2-methoxyphenyl)malonateHCID 86698720—

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 4-bromo-1-iodo-2-methoxybenzene (1100 mg, 3.5 mmol), diethylmalonate (1240 mg, 7.70 mmol), cesium carbonate (1830 mg, 5.60 mmol), 2-picolinic acid (62 mg, 0.39 mmol), copper (I) iodide (34 mg, 0.18 mmol), and dioxane (7 ml) was stirred at 55° C. for 2 days. A very heavy slurry formed, LCMS indicates that the starting iodoarene is about 70% consumed. The mixture was cooled to room temperature and diluted with 30 mL of water and extracted with ethyl acetate. The extract was washed with water, brine, dried over magnesium sulfate, and concentrated to obtain the title compound which was about 60% pure by LCMS and was used for the next step without purification. GCMS (ES+) 344 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394285B2
Source datasetuspto-grants-2016_07
ORD IDord-38b3b7a36d8e469bbab438dd1175e3be
Source noteuspto-grants-2016_07