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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338378Generated: October 30, 2026

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

https://huagongshe.com/reaction/338378

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 numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-bf02ec484bdb44c7a80c1d9c839dfa0f
Source noteuspto-grants-2014_11