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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488667Generated: October 26, 2026

Methyl Acrylate → 3-(4-Amino-1-naphthyl)propanoic acid

https://huagongshe.com/reaction/488667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
Reactant4-Bromo-1-naphthylamineHCID 75303—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantPotassium AcetateHCID 517044—
Catalystpalladium(II) acetateHCID 167845—
CatalystTetrabutylammonium chloride hydrateHCID 16212273—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-(4-Amino-1-naphthyl)propanoic acidHCID 2227193058.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 4-bromo-1-naphthylamine (4.44 g, 20.0 mmol), potassium acetate (6.28 g, 64.0 mmol), tetrabutylammonium chloride hydrate (6.1 g, 22 mmol), palladium(II)acetate (224 mg, 1.0 mmol) and tri-o-tolylphosphine (1.22 g, 4.0 mmol) was added DMF (60 mL) and methyl acrylate (2.3 mL, 25 mmol). The reaction was heated to 100° C. under N2 for 2 hours, poured into water (300 mL) and extracted with diethyl ether (3×50 mL). The combined ether layers were washed with brine (1×50 mL), dried (MgSO4), filtered, and concentrated under reduced pressure. The product was purified on silica gel eluting with 30% ethyl acetate/hexanes to provide the titled compound 2.5 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06972340B2
Source datasetuspto-grants-2005_12
ORD IDord-67cb650aaed443c6be9a79aeee2a1e7e
Source noteuspto-grants-2005_12