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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541149Generated: October 25, 2026

Citric Acid → 2-(5-Methoxy-pyridin-2-yl)-benzoic acid diethylamide

https://huagongshe.com/reaction/541149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(2-(Diethylcarbamoyl)phenyl)boronic acidHCID 4190636—
Reactant2-Chloro-5-methoxypyridineHCID 15169000—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product2-(5-Methoxy-pyridin-2-yl)-benzoic acid diethylamideHCID 5949278728.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

Under an argon atmosphere, a mixture of tripotassium phosphate (6.24 g) and water (15 ml) was added to a mixture of 2-chloro-5-methoxy-pyridine (2.05 g), 2-(diethylcarbamoyl)benzeneboronic acid (4.65 g), 1,1′-bis(diphenylphosphino)ferrocene-palladium(II) dichloride-dichloromethane complex (0.584 g) and toluene (30 ml), and the mixture was stirred at 80° C. for 2 hr. The reaction mixture was cooled to room temperature, water (20 ml), citric acid (2.2 g) and ethyl acetate were added and the mixture was stirred and filtered through celite. The filtrate was partitioned in a separatory funnel. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure and the obtained residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/1 to 1/2) to give a roughly purified product (1.144 g) of the title compound. This product was directly used for the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871934B2
Source datasetuspto-grants-2014_10
ORD IDord-996e065bbc964b5c82d86c73e3dba0a9
Source noteuspto-grants-2014_10