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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6738Generated: October 26, 2026

2-(2-Aminoethyl)-5-methoxyindole → 6-Hydroxytryptamine

https://huagongshe.com/reaction/6738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Aminoethyl)-5-methoxyindoleHCID 17654—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTolueneHCID 1140—
Product6-HydroxytryptamineHCID 16046368.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Diisobutylaluminum hydride (1 M in toluene, 15 mL) was slowly added to a suspension of 2-(6-methoxy-1H-indol-3-yl)ethylamine (250 mg) in 20 mL of toluene. The resulting clear solution was refluxed for 10 h, then cooled to 0° C. and quenched by the careful addition of 20 mL of 1:1 methyl alcohol:water. The mixture was stirred for 15 min at rt and filtered to remove the precipitated aluminum salts. The solvent was evaporated to yield 158 mg of 3-(2-amino-ethyl)-1H-indol-6-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084154B2
Source datasetuspto-grants-2006_08
ORD IDord-e5c557f7a27d4624a1960146dfa584ae
Source noteuspto-grants-2006_08