Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5599Generated: October 23, 2026

Indole → 1-(Allyl)-1H-indole

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantAllyl bromideHCID 7841—
Reactant18-Crown-6HCID 28557—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product1-(Allyl)-1H-indoleHCID 8562574%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05245046
Source datasetuspto-grants-1993_09
ORD IDord-a27889ee44e040db9dcdb94b80457c09
Source noteuspto-grants-1993_09