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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7067Erstellt: 23. Oktober 2026

Triethylamine → 4-Hydroxy-3-methoxy-n-[3-[2-(2-trifluoromethylphenyl)ethynyl]phenyl]phenylacetamide

https://huagongshe.com/de/reaction/7067

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktBenzene, 1-iodo-2-(trifluoromethyl)-HCID 67957—
EduktN-(3-ethynylphenyl)-4-hydroxy-3-methoxyphenyacetamideHCID 86760178—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178419050HCID 178419050—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-Hydroxy-3-methoxy-n-[3-[2-(2-trifluoromethylphenyl)ethynyl]phenyl]phenylacetamideHCID 12096663—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A mixture of N-(3-ethynylphenyl)-4-hydroxy-3-methoxypheny-acetamide (the compound of Example 19) (200 mg), 1-trifluoromethyl-2-iodobenzene (280 mg), copper (I) iodide (19 mg), bis(triphenylphosphine)palladium (II) dichloride (70 mg), triethylamine (1 g) and acetonitrile (3 ml) is heated with stirring at 50° C. under argon atmosphere for 18 hours. The solvent is evaporated under reduced pressure, and the residue is purified by silica gel column chromatography (eluent: gradient from 0% to 100% hexane/ethyl acetate) to give the desired compound (120 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084176B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-b5a3ba4d153e4ab996f6b3ba98b5134c
Quellennotizuspto-grants-2006_08