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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636193Generated: November 4, 2026

Indole → 1-Octyl-1H-indole

https://huagongshe.com/reaction/1636193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
Reactant1-BromooctaneHCID 8140—
ReactantPotassium HydroxideHCID 14797—
Catalyst18-Crown-6HCID 28557—
SolventBenzeneHCID 241—
Product1-Octyl-1H-indoleHCID 1282727372.3%

Reaction Steps

A mixture of indole (1) (0.03 mole, 3.51 g), potassium hydroxide (0.03 mole, 1.97 g) powdered in a mortar, and 18-crown-6 ether (0.001 mole, 250 mg) in benzene (20 cm3) is heated under reflux with vigorous stirring for two hours. A solution of octylbromide (2a), (0.04 mole, 7.72 g) in benzene (10 cm3) is added and reflux is maintained for an additional four hours. The reaction is monitored by TLC and the reaction mixture is filtered on Celite. Evaporation of the solvent yields an orange liquid which is purified by distillation in vacuo. The colourless liquid distilled at 154-156° C. and 1.5 mmHg pressure is shown by 1H nmr to be pure 1-octylindole (3a) (4.98 g, 0.0217 mole, 72% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06033601
Source datasetuspto-grants-2000_03
ORD IDord-3bbccff0c1224cf0bd606ae94d1e0e46
Source noteuspto-grants-2000_03