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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043669Generated: November 1, 2026

Ethyl Acetate → Methyl 2-(2,4-dimethoxyphenyl)-5-nitrobenzoate

https://huagongshe.com/reaction/1043669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
ReactantMethyl 2-Bromo-5-nitrobenzoateHCID 245494—
Reactant2,4-Dimethoxybenzeneboronic acidHCID 2734341—
CatalystHCID 178419050HCID 178419050—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(2,4-dimethoxyphenyl)-5-nitrobenzoateHCID 57990576—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2,4-dimethoxyphenylboronic acid (25.0 g, 137 mmol), methyl 2-bromo-5-nitrobenzoate (35.7 g, 137 mmol), cesium carbonate (89.4 g, 274 mmol) and bis(triphenylphosphine)palladium (II) dichloride (4.81 g, 6.85 mmol) was suspended in N,N-dimethylformamide (450 mL), and then the suspension was stirred under argon atmosphere at 80° C. overnight. After cooling down, ethyl acetate (200 mL), diethylether (400 mL) and water (1000 mL) were added thereto and the mixture was separated into a water phase and an organic layer. The water layer was extracted with a mixed solvent of ethyl acetate (150 mL)-diethylether (150 mL) (twice). The combined organic layer was washed with water (500 mL, 3 times) and saturated brine (500 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure to give the titled reference compound as a brown oil. (Quantitative)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563551B2
Source datasetuspto-grants-2013_10
ORD IDord-f21fadbd4674424b885ffca0e7fa6d90
Source noteuspto-grants-2013_10