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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5599생성일: 2026년 10월 23일

Indole → 1-(Allyl)-1H-indole

https://huagongshe.com/ko/reaction/5599

반응식

참여 물질

역할이름HCID투입량
반응물IndoleHCID 798—
반응물Allyl bromideHCID 7841—
반응물18-Crown-6HCID 28557—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물1-(Allyl)-1H-indoleHCID 8562574%

반응 단계

To a solution of 2.39 g (9.04 mmoles) of 18-crown-6 in 250 ml of dry ether was added 13.1 g (116.7 mmoles) of potassium tert-butoxide. The mixture was stirred while 11.72 g (100 mmoles) indole was added. The stirring was continued for 3 hours. All of the solid did not dissolve. Then 14.1 g (116.5 mmoles) of allyl bromide in 100 ml of ether was added during 0.5 hour. The stirring was continued for 67.5 hours. Water (200 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 16.02 g of brown oil. The oil was chromatographed on a 1100 g column of silica gel. The column was eluted with 10% acetone-Skellysolve B and 2200 ml fractions were collected. The fractions were assayed by silica gel tlc (1×4") (10% acetone-Skellysolve B). Fractions 17-23 were combined giving 11.60 g (74%) of 1-allylindole as a yellow brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245046
출처 데이터셋uspto-grants-1993_09
ORD IDord-a27889ee44e040db9dcdb94b80457c09
출처 메모uspto-grants-1993_09