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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265085Generated: October 27, 2026

Ethyl Acrylate → Ethyl 3-(4-amino-2-fluorophenyl)prop-2-enoate

https://huagongshe.com/reaction/2265085

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 3-(4-amino-2-fluorophenyl)prop-2-enoateHCID 5398718776%

Reaction Conditions

Temperature110 °C

Reaction Steps

4-Bromo-3-fluoroaniline (5.0 g) was dissolved in a mixed solvent of DMF (18 ml) and N,N-diisopropylethylamine (18 ml). Ethyl acrylate (3.9 ml), palladium acetate (295 mg), and tris(2-methylphenyl) phosphine (3.2 g) were added to the obtained mixture in a nitrogen atmosphere, and the mixture was stirred at 110° C. for 5 hours. The reaction mixture was filtered through Celite and separated with ethyl acetate and water. The organic layer was washed with a saturated sodium chloride solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by neutral silica gel column chromatography (14-25% ethyl acetate/n-hexane). The purified material was crystallized with n-hexane to obtain Compound 2a (4.2 g, 76%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855300B2
Source datasetuspto-grants-2010_12
ORD IDord-988024a7cabc462ca6d8a5bc74051e8d
Source noteuspto-grants-2010_12