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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 604413Erstellt: 27. Oktober 2026

HCID 178418260, Verbindung → HCID 178470417, Verbindung

https://huagongshe.com/reaction/604413

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHCID 178418260HCID 178418260—
EduktHCID 178470418HCID 178470418—
KatalysatorFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
KatalysatorTetraethylammonium cyanideHCID 3014735—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 178470417HCID 178470417—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

1.57 g (4.5 mmol) of 4-Iodo-5-thiophen-2-yl-2H-pyrazole-3-carboxylic acid ethyl ester, 0.81 g (9.0 mmol) of copper cyanide and 352 mg (2.3 mmol) of tetraethylammonium cyanide were dissolved in 10 ml of DMF and 20 ml of tetrahydrofuran and the solution was degassed with argon. 223 mg (0.2 mmol) of Tris(dibenzylideneacetone)dipalladium (0) and 374 mg (0.7 mmol) of 1,1′-bis-(diphenylphosphino) ferrocene were added at RT. The reaction was stirred at 120° C. for 5 h. The solvent was removed under reduced pressure. The residue was dissolved in ethyl acetate and this solution was washed with saturated aqueous sodium bicarbonate. The organic phase was dried with sodium sulfate, filtered and the solvent was removed under reduced pressure. The product was purified by silica gel chromatography eluting with n-heptane:ethyl acetate/1:1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07910606B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-d5aca9ab470340549bb7eda1ac3675c9
Quellennotizuspto-grants-2011_03