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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507916Generated: November 3, 2026

Ethyl Acrylate → ethyl(2E)-3-(4-amino-2-fluorophenyl)acrylate

https://huagongshe.com/reaction/507916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant4-Bromo-3-fluoroanilineHCID 821848—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
SolventDiisopropylethylamineHCID 81531—
Productethyl(2E)-3-(4-amino-2-fluorophenyl)acrylateHCID 2053650696%

Reaction Conditions

Temperature110 °C

Reaction Steps

4-Bromo-3-fluoroaniline (13.3 g, 70.0 mmol), ethyl acrylate (9.48 mL, 87.5 mmol) and tris(2-methylphenyl)phosphine (8.52 g, 28.0 mmol) were dissolved in N,N-diisopropylethylamine (50 mL) and N,N-dimethylformamide (50 mL), palladium(II) acetate (0.786 g, 3.50 mmol) was added, and the mixture was stirred under an argon atmosphere at 110° C. for 5 hr. After cooling the reaction mixture, the solvent was evaporated under reduced pressure. Water and ethyl acetate were added to the residue, and the insoluble material was removed by filtering through celite. The organic layer in the filtrate was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (20%-60% ethyl acetate/hexane) to give the title compound (14.0 g, yield 96%). A part thereof was recrystallized to give yellow prism crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786165B2
Source datasetuspto-grants-2010_08
ORD IDord-0ce3e775f2064b1d9ecdac16989cae66
Source noteuspto-grants-2010_08