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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6948Erstellt: 24. Oktober 2026

Benzyl Chloride → 1,1-di-(N-benzyl-indol-3-yl)-butane

https://huagongshe.com/de/reaction/6948

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl ChlorideHCID 7503—
Edukt3-[1-(1H-indol-3-yl)butyl]-1H-indoleHCID 10266133—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelChloroform waterHCID 22418719—
Produkt1,1-di-(N-benzyl-indol-3-yl)-butaneHCID 2201929978%

Reaktionsschritte

ST 1385 1,1-di-indol-3-yl-butane, 290 mg (1 mmol), was thoroughly mixed and blended with potassium tertbutylate (280 mg) and tetrabutylammonium bromide (20 mg). The mixture thus obtained was held under ultrasonic stirring at ambient temperature. 640 mg (5 mmol) of benzylchloride at 0° C. were then added and the ultrasonic stirring was continued for 2 hours at room temperature. At the end of this period, the reaction mixture was treated with H2O/CHCl3; the chloroform phase was separated, washed with a small amount of water, dried on Na2SO4, filtered and concentrated to dryness. The end product was isolated and purified chromatographically on silica gel, eluting with hexane:ethyl ether 95:5.351 mg of product were obtained with a 78% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07084166B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-4dd0bc4fe8c64d9e8f8801e446e2f232
Quellennotizuspto-grants-2006_08