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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5596생성일: 2026년 10월 23일

Benzyl Bromide → 1-Benzyl-5-chloro-1H-indole

https://huagongshe.com/ko/reaction/5596

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물18-Crown-6HCID 28557—
반응물5-ChloroindoleHCID 87110—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물1-Benzyl-5-chloro-1H-indoleHCID 1847636290%

반응 단계

To a solution of 0.8 g (3.03 mmoles) of 18-crown-6 in 100 mL of dry ether was added 4.39 g (39.12 mmoles) potassium tert-butoxide. The mixture was stirred while 5.08 g (33.51 mmoles) of 5-chloroindole was added. The stirring was continued for 0.5 hour. Most of the solid dissolved. Then 6.69 g (39.11 mmoles) of benzyl bromide in 40 mL of ether was added during 0.5 hours. The stirring was continued for 27 hours. Water (100 mL) was added. The layers were separated. The aqueous layer was extracted with ether (2×75 mL). The combined ether phases were washed with 50 mL of brine and dried over MgSO4. Evaporation of the solvent left 9.17 g of orange oil. The oil was chromatographed on a 700 g column of silica gel. The column was eluted with 1:2 CH2Cl2 -Skellysolve B and 200 mL fractions were collected. The fractions were assayed by silica gel tlc (2×8") (1:2 CH2Cl2 -Skellysolve B). Fractions 10-14 were combined giving 7.26 g (90%) of 1-benzyl-5-chloroindole as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245046
출처 데이터셋uspto-grants-1993_09
ORD IDord-0121012381ad40bb9bdeb58d7a76e8eb
출처 메모uspto-grants-1993_09