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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353471Generated: October 29, 2026

Indole → 1-Octyl-1H-indole

https://huagongshe.com/reaction/353471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantWaterHCID 962—
Reactant1-BromooctaneHCID 8140—
ReactantSodium hydrideHCID 24758—
SolventDimethyl SulfoxideHCID 679—
Product1-Octyl-1H-indoleHCID 12827273—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of indole (1.0 g) in dry DMSO (1 ml) is dropped into a suspension of sodium hydride (60% mineral oil suspension; 0.37 g) in dry DMSO (20 ml). The mixture is heated at 60° C. for 1 h. After cooling to room temperature, the resulting solution is added dropwise with a solution of n-octyl bromide (2.82 ml) in dry DMSO (2.8 ml). After a night at room temperature, the reaction mixture is poured into water (200 ml) and extracted with ethyl acetate (2×50 ml). The combined organic phases are washed with a NaCl saturated solution, dried and evaporated to dryness. The resulting residue is purified by column chromatography (silica gel; eluent n-hexane), to obtain 1.86 g of 1-(n-octyl)indole as oil. The compound is characterized through its 1H-NMR spectrum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06753342B2
Source datasetuspto-grants-2004_06
ORD IDord-52c060f459ff4a34807b3553e00c2657
Source noteuspto-grants-2004_06