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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254177Generated: November 2, 2026

6-Nitro-1H-indole → 6-Aminoindole

https://huagongshe.com/reaction/2254177

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Nitro-1H-indoleHCID 78502—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product6-AminoindoleHCID 256096—

Reaction Steps

A yellow solution of 5.2 g. 6-nitroindole in 150 ml. ethyl acetate was added to 1.25 g. of pre-induced 10% w/w palladium-on-charcoal in 50 ml. ethyl acetate. The mixture was shaken under 3.45 bar hydrogen overnight and then filtered through diatomaceous earth. The residue was washed with 150 ml. hot chloroform and the combined colourless filtrate and washings were evaporated to give a quantitative yield of 6-aminoindole as a dark oil; NMR: 3.5 (br s, 2H, NH2), 6.4 (m, 1H, H3). 6.5 (m, 2H, H5 +H7), 7.0 (dd, 1H, H2, 7.4 (d, 1H, H4), 7.8 (br, 1H, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05234942
Source datasetuspto-grants-1993_08
ORD IDord-eaafb538597c4246a869562785facd29
Source noteuspto-grants-1993_08