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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6948생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl ChlorideHCID 7503—
반응물3-[1-(1H-indol-3-yl)butyl]-1H-indoleHCID 10266133—
촉매Tetrabutylammonium BromideHCID 74236—
용매Chloroform waterHCID 22418719—
생성물1,1-di-(N-benzyl-indol-3-yl)-butaneHCID 2201929978%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084166B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-4dd0bc4fe8c64d9e8f8801e446e2f232
출처 메모uspto-grants-2006_08