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HRID 6948作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl ChlorideHCID 7503—
反応物3-[1-(1H-indol-3-yl)butyl]-1H-indoleHCID 10266133—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒Chloroform waterHCID 22418719—
生成物1,1-di-(N-benzyl-indol-3-yl)-butaneHCID 2201929978%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084166B2
出典データセットuspto-grants-2006_08
ORD IDord-4dd0bc4fe8c64d9e8f8801e446e2f232
出典メモuspto-grants-2006_08