Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 43356Erstellt: 23. Oktober 2026

Methyl Acrylate → Ethyl (2E)-3-(5-formyl-2-pyridinyl)-2-propenoate

https://huagongshe.com/de/reaction/43356

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl AcrylateHCID 7294—
EduktTri-o-tolylphosphineHCID 80271—
EduktSodium AcetateHCID 517045—
Edukt6-Bromo-3-pyridinecarboxaldehydeHCID 11769234—
KatalysatorPalladium, di-mu-chlorobis(eta3-2-propenyl)di-HCID 61538—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl (2E)-3-(5-formyl-2-pyridinyl)-2-propenoateHCID 8662816093,7%

Reaktionsbedingungen

Temperatur170 °C

Reaktionsschritte

A mixture of 2-bromo-5-formylpyridine (500 mg, 2.6 mmol), methyl acrylate (0.6 ml, 6.5 mmol), tri-(o-tolyl)phosphine (80 mg, 0.26 mmol), allyl palladium (II) chloride dimer (47 mg, 0.13 mmol) and sodium acetate (1.08 g, 8 mmol) in DMF (10 ml) was heated at 170° C. in a microwave reactor for 0.75 h. The reaction mixture was filtered through Celite® then diluted with DCM and water. The organic phase was dried, concentrated in vacuo and purified by chromatography to give the title compound as a white solid (50 mg). δH (CDCl3, 250 MHz) 10.14 (1H, s), 9.09 (1H, d), 8.19 (1H, dd), 7.72 (1H, d), 7.57 (1H, d), 7.08 (1H, d), 3.85 (3H, s). MS (ES): MH+ 192.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536182B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-c0809180160c4ca9954d8ce9512a8b6f
Quellennotizuspto-grants-2013_09