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HRID 5599作成日:2026年10月23日

Indole → 1-(Allyl)-1H-indole

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

反応式

関与物質

役割名称HCID仕込み量
反応物IndoleHCID 798—
反応物Allyl bromideHCID 7841—
反応物18-Crown-6HCID 28557—
反応物Potassium tert-butoxideHCID 23665647—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物1-(Allyl)-1H-indoleHCID 8562574%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05245046
出典データセットuspto-grants-1993_09
ORD IDord-a27889ee44e040db9dcdb94b80457c09
出典メモuspto-grants-1993_09