Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 226357Erstellt: 27. Oktober 2026

Ethyl Acrylate → ethyl (2E)-3-(6-bromo-5-methyl-3-pyridyl)acrylate

https://huagongshe.com/reaction/226357

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcrylateHCID 8821—
EduktTri-o-tolylphosphineHCID 80271—
EduktDiisopropylethylamineHCID 81531—
Edukt2-Bromo-5-iodo-3-methylpyridineHCID 10108680—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produktethyl (2E)-3-(6-bromo-5-methyl-3-pyridyl)acrylateHCID 86603663—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a solution of 2-bromo-5-iodo-3-methylpyridine (1.5 g) in DMF (15 mL) was added palladium(II) acetate (56.5 mg) and tri-o-tolylphosphine (230 mg) and diisopropylethylamine (3.5 mL), and ethyl acrylate (1.09 mL). The mixture was heated at 90° C. for 1 hour. Resulting mixture was poured into water and extracted with AcOEt. The organic layer was washed with water and brine, and dried over Na2SO4, and the solvent was removed in vacuo. Residual brown oil was purified by silica gel column chromatography eluted with AcOEt and hexane (1:4-1:2) to give ethyl (2E)-3-(6-bromo-5-methyl-3-pyridyl)acrylate (1.00 g) as pale yellow powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07557127B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-1526812b5b584f43bb9038b3b0fb20ce
Quellennotizuspto-grants-2009_07