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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364571Generated: October 26, 2026

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

https://huagongshe.com/reaction/2364571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantTriethylamineHCID 8471—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant2-Bromo-5-fluoroanilineHCID 2773317—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product(E)-Methyl 3-(2-amino-4-fluorophenyl)acrylateHCID 2300331351%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 2-bromo-5-fluoroaniline (35.00 g, 184 mmol, Aldrich), palladium (II) acetate (2.06 g, 9.18 mmol, Strem) and tri(o-tolyl)phosphine (5.60 g, 18.40 mmol; Strem) in acetonitrile (350 ml) at RT was added methyl acrylate (33.00 ml, 365 mmol, Aldrich) and triethylamine (64.00 ml, 460 mmol, Aldrich). The reaction was heated at 80° C. for 24 h. The reaction mixture was diluted with EtOAc (500 mL) and the resulting colorless crystalline solid was filtered and washed with EtOAc. The organic solution was concentrated to dryness and the solids were slurried in 10% EtOAc/hexane at 60° C. for 1 h. The slurry was cooled to RT and filtered. The solid was washed with 10% EtOAc/hexane and sucked dry with air to give 18.30 g (51%) of a light-yellow crystalline solid. m/z=195.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691986B2
Source datasetuspto-grants-2014_04
ORD IDord-f535b760ff3f48e09063e865c9ebec65
Source noteuspto-grants-2014_04