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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1198562Erstellt: 23. Oktober 2026

Potassium Carbonate → 7-(Cyanomethoxy)indole

https://huagongshe.com/de/reaction/1198562

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktBromoacetonitrileHCID 11534—
Edukttrans-3-[2-(7-Chloroquinolin-2-yl)ethenyl]benzyl alcoholHCID 10827738—
KatalysatorPalladium hydroxideHCID 9942167—
LösungsmittelMethanolHCID 887—
LösungsmittelTolueneHCID 1140—
Produkt7-(Cyanomethoxy)indoleHCID 15054020—

Reaktionsschritte

The protected 7-substituted indole (Example 34a part ii) (0.53 g, 1.75 mmol) in methanol (10 ml) and toluene (10 ml) was hydrogenated in a Parr apparatus at 50 p.s.i. for 1 hour in the presence of Pearlman's catalyst (0.33 g). The reaction mixture was filtered through Celite and the filtrate evaporated in vacuo. The crude 7-hydroxy indole was taken up in methyl ethyl ketone (20 ml), and bromoacetonitrile (0.65 g, 5.25 mmol) and anhydrous potassium carbonate (0.6 g, 4.35 mmol) added. The mixture was refluxed under nitrogen for 1 hour, cooled, poured into 2.5M hydrochloric acid/ice and extracted into dichloromethane. The organic phase was washed with water, dried, filtered and evaporated in vacuo.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05281593
Quelldatensatzuspto-grants-1994_01
ORD IDord-cfb28e7ed3b24622adf9dc9b1f6170ad
Quellennotizuspto-grants-1994_01