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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 347322Erstellt: 25. Oktober 2026

Diisopropylamine → [4-(3-Methoxyprop-1-ynyl)benzofuran-7-yl]amine

https://huagongshe.com/reaction/347322

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
EduktEthyl AcetateHCID 8857—
Edukt4-Iodo-7-benzofuranamineHCID 21082723—
KatalysatorCopper iodideHCID 83717—
KatalysatorHCID 178418476HCID 178418476—
Produkt[4-(3-Methoxyprop-1-ynyl)benzofuran-7-yl]amineHCID 21082722—

Reaktionsschritte

Bis(Triphenyl-phosphine)palladium(II) chloride (144 mg), copper iodide (58 mg) and diisopropylamine (208 mg) were added to a stirred solution of (4-Iodo-7-amino-benzfuran) (266 mg) and methyl propargyll ether (144 mg) in ethyl acetate (5 mls) at −20° C. The reaction was allowed to warm to ambient temperature over 16 hours. The reaction mixture was partitioned between ethyl acetate and saturated NaHCO3. The organics were washed with saturated NaHCO3, water and saturated brine and dried over magnesium sulfate. The product was purified by column chromatography on silica using 100% dichloromethane as eluent. [4-(3-methoxyprop-1-ynyl)benzofuran-7-yl]amine was thus obtained as a yellow/brown gum (70 mg); NMR Spectrum: (DMSOd6) 3.34 (s, 3H), 4.34 (s, 2H), 5.74 (s, 2H), 6.50 (d, 1H), 6.80 (s, 1H), 7.05 (d, 1H), 7.96, s, 1H); Mass Spectrum: M+H+ mass ion not observed.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07173136B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-37ac8b37f06a473e8e4a73313b8c8d6c
Quellennotizuspto-grants-2007_02