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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691530Generated: November 2, 2026

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

https://huagongshe.com/reaction/1691530

Reaction equation

Participants

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

Reaction Conditions

Temperature110 °C

Reaction Steps

To a mixture of 4-bromo-3-fluoroaniline (13.3 g, 70.0 mmol), ethyl acrylate (9.48 mL, 87.5 mmol), tris(2-methylphenyl)phosphine (8.52 g, 28.0 mmol), N,N-diisopropylethylamine (50 mL) and N,N-dimethylformamide (50 mL) was added palladium(II) acetate (0.786 g, 3.50 mmol), and the mixture was stirred at 110° C. for 5 hr under an argon atmosphere. The reaction mixture was cooled, and the solvent was evaporated under reduced pressure. Water and ethyl acetate were added to the residue, and the insoluble material was filtered off through celite. The filtrate was separated into the aqueous layer and the organic layer. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=20:80-60:40) to give the title compound (14.0 g, yield 96%). A part thereof was recrystallized to give yellow prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153694B2
Source datasetuspto-grants-2012_04
ORD IDord-cf911990dea34769a75ea450d45865bd
Source noteuspto-grants-2012_04