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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226392Generated: October 27, 2026

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

https://huagongshe.com/reaction/226392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-5-iodopyrimidineHCID 1714223—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductEthyl (E)-3-(2-chloropyrimidin-5-yl)acrylateHCID 53259409—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 2-chloro-5-iodopyrimidine (7.62 g), palladium(II) acetate (356 mg), tri(o-tolyl)phosphine (965 mg), and DMF (32 mL) was added ethyl acrylate (17.2 mL) and N,N-diisopropylethylamine (13.8 mL). After stirring for 3 hours at 100° C., the reaction mixture was partitioned between ethyl acetate and H2O. The organic layer was dried over MgSO4, filtered, and evaporated in vacuo. The residue was purified by column chromatography on silica gel to give ethyl (2E)-3-(2-chloro-5-pyrimidinyl)acrylate (2.32 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-b212646e797944888b766c08bba54603
Source noteuspto-grants-2009_07