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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385572Generated: October 30, 2026

Water → butyl (2E)-3-(3-amino-5-fluoropyridin-2-yl)acrylate

https://huagongshe.com/reaction/385572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantButyl AcrylateHCID 8846—
ReactantEthyl AcetateHCID 8857—
Reactant2-Chloro-5-fluoropyridin-3-amineHCID 44754868—
CatalystHCID 178418851HCID 178418851—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Productbutyl (2E)-3-(3-amino-5-fluoropyridin-2-yl)acrylateHCID 68105236—

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of 150 g of 2-chloro-5-fluoropyridin-3-amine in 600 mL of N,N-dimethylformamide, 190 mL of butyl acrylate and 287 mL of triethylamine were added under a nitrogen flow, and the mixture was stirred at 110° C. for 2 hours. The reaction mixture was cooled to 58° C., thereto were added 13.1 g of bis(tri-tert-butylphosphine)palladium(0), and the mixture was stirred at 110 to 120° C. for 40 minutes. The reaction mixture was cooled to 57° C., 13.1 g of bis(tri-tert-butylphosphine)palladium(0) was added thereto, and the mixture was stirred at 110 to 120° C. for 3 hours. The reaction mixture was cooled to room temperature, and water and ethyl acetate were added thereto. The insoluble substance was filtered off, the organic layer of the filtrate was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed sequentially with water and a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Cyclohexane and ethyl acetate were added to the resultant residue, and the solid was filtered off to obtain 200 g of butyl (2E)-3-(3-amino-5-fluoropyridin-2-yl)acrylate as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367831B2
Source datasetuspto-grants-2013_02
ORD IDord-76ddfe707f124265a876f15d28a8f3a9
Source noteuspto-grants-2013_02