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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5601생성일: 2026년 10월 23일

Benzyl Chloride → 1-Benzyl-5-fluoro-1H-indole

https://huagongshe.com/ko/reaction/5601

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl ChlorideHCID 7503—
반응물18-Crown-6HCID 28557—
반응물5-FluoroindoleHCID 67861—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물1-Benzyl-5-fluoro-1H-indoleHCID 1979663914.1%

반응 단계

To a solution of 0.8 g (3.03 mmoles) of 18-crown-6 in 100 ml of dry ether was added 3.27 g (29.14 mmoles) of potassium tert-butoxide. The mixture was stirred while a solution of 3.75 g (27.75 mmoles) of 5-fluoroindole in 80 ml of ether was added. The stirring was continued for 0.5 hour. Solid was present. Then 3.69 g (29.15 mmoles) of benzyl chloride in 80 ml of ether was added. The mixture was stirred for 28 hours. Water (100 ml) was added. The layers were separated. The aqueous layer was extracted with 100 ml of ether. The combined ether layers were washed with 50 ml of brine and dried over MgSO4. Evaporation of the solvent left 6.95 g of orange oil. The oil was chromatographed on a 600 g column of silica gel. The column was eluted with 30% CH2Cl2 -Skellysolve B and 200 ml fractions were collected. The fractions were assayed by silica gel tlc (1×4") (30% CH2Cl1 -Skellysolve B). Fractions 11-15 were combined giving 0.88 g (14%) of 1-benzyl-5-fluoroindole as a pale yellow oil which contained a small amount of 1,3-dibenzyl-5-fluorindole.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245046
출처 데이터셋uspto-grants-1993_09
ORD IDord-d0c9152d9e564c87bc2c916dccd31853
출처 메모uspto-grants-1993_09