Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 59113Erstellt: 23. Oktober 2026

tert-Butyl methyl ether → Methyl 2-chloro-6-(1-ethoxyvinyl)pyrimidine-4-carboxylate

https://huagongshe.com/de/reaction/59113

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl methyl etherHCID 15413—
EduktMethyl 2,4-dichloropyrimidine-6-carboxylateHCID 239689—
EduktPotassium FluorideHCID 522689—
EduktStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 2-chloro-6-(1-ethoxyvinyl)pyrimidine-4-carboxylateHCID 11782140475%

Reaktionsbedingungen

Temperatur94 °C

Reaktionsschritte

Methyl 2,6-dichloropyrimidine-4-carboxylate (8.44 g, 40.77 mmol) and bis(triphenylphosphine)-palladium(II) chloride (0.572 g, 0.82 mmol) in DMF (80 mL) was degased. Tributyl(1-ethoxy-vinyl)tin (14.46 mL, 42.81 mmol) was added under argon. The mixture was heated at 94° C. for 1 h. The mixture was poured into a solution of potassium fluoride (30 g) in water (400 mL). MTBE (300 mL) was added and the mixture was stirred for 10 min. The mixture was filtered and the filter was washed with 200 mL of MTBE. The filtrate was washed with brine (100 mL), dried over sodium sulfate and the solvents were evaporated. The residue purified by column chromatography on silica eluting with DCM to give the title compound as a solid (7.40 g, 75%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09439904B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-04fc7098ba644efc9570b0c89b16e660
Quellennotizuspto-grants-2016_09