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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6948Generated: October 26, 2026

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

https://huagongshe.com/reaction/6948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
Reactant3-[1-(1H-indol-3-yl)butyl]-1H-indoleHCID 10266133—
CatalystTetrabutylammonium BromideHCID 74236—
SolventChloroform waterHCID 22418719—
Product1,1-di-(N-benzyl-indol-3-yl)-butaneHCID 2201929978%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084166B2
Source datasetuspto-grants-2006_08
ORD IDord-4dd0bc4fe8c64d9e8f8801e446e2f232
Source noteuspto-grants-2006_08