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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 330821Erstellt: 24. Oktober 2026

Tributylamine → HCID 66691768, Verbindung

https://huagongshe.com/de/reaction/330821

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributylamineHCID 7622—
EduktEthyl AcetateHCID 8857—
Edukt3,3-Diethoxy-1-propeneHCID 62477—
EduktHCID 66691575HCID 66691575—
KatalysatorTetrabutylammonium ChlorideHCID 70681—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 66691768HCID 66691768—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

To 1.80 g (5.17 mmol) 1-ethoxy-4-((4-iodophenyl)ethynyl)benzene (XII.1) in 24 mL DMF are added 2.36 mL (15.5 mmol) 3,3-diethoxy-propene, 3.69 mL (15.5 mmol) tributylamine, 1.44 g (5.17 mmol) tetrabutylammoniumchloride and 0.04 g (0.16 mmol) palladium(II)acetate under argon. The mixture is stirred at 120° C. for 12 h. After that time, 1.18 mL (7.76 mmol) 3,3-diethoxy-propene are added and the mixture is stirred at 120° C. for 5 d. After cooling, EtOAc is added and the mixture is washed with 1N potassium hydrogensulfate solution and water. The organic layer is dried over sodium sulphate and the solvent is evaporated. The residue is purified by column chromatography (silica gel; PE:DCM 1:1) to yield the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08877754B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-caeaae0a8b5941e9b57e00af235f045f
Quellennotizuspto-grants-2014_11