Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226460Generated: October 27, 2026

Ethyl Acrylate → Ethyl (E)-3-(2-chloropyrimidin-5-yl)acrylate

https://huagongshe.com/reaction/226460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductEthyl (E)-3-(2-chloropyrimidin-5-yl)acrylateHCID 53259409—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 5-bromo-2-chloropyrimidine (500 mg) in DMF (5 mL) was added ethyl acrylate (1.41 mL), palladium(II) acetate (29 mg), tris(2-methylphenyl)phosphine (118 mg), and N,N-diisopropylethylamine (1.35 mL). The mixture was stirred at 100° C. for 4 hours. The resulting mixture was allowed to cool to ambient temperature, poured into brine, and extracted with ethyl acetate. The organic phase was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with a mixture of hexane and ethyl:acetate (90:10 v/v) to give ethyl (2E)-3-(2-chloro-5-pyrimidinyl)acrylate (494 mg) as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-b789b3bdb6bf4be48891d65d57b6b91a
Source noteuspto-grants-2009_07