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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403982Generated: October 25, 2026

(E)-2-(5-fluoro-2,4-dinitrophenyl)-N,N-dimethylethenamine → 5-Fluoro-1H-indol-6-amine

https://huagongshe.com/reaction/1403982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-2-(5-fluoro-2,4-dinitrophenyl)-N,N-dimethylethenamineHCID 15022335—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product5-Fluoro-1H-indol-6-amineHCID 1502233621.5%

Reaction Steps

A suspension of (E)-2-(5-fluoro-2,4-dinitrophenyl)-N,N-dimethylethenamine (8.0 g, 31 mmol) and Raney Nickel (8 g) in EtOH (80 mL) was stirred under H2 (40 psi) at room temperature for 1 h. After filtration, the filtrate was concentrated and the residue was purified by column chromatography (petroleum ether/ethyl acetate=5/1) to give 5-fluoro-1H-indol-6-amine (1.0 g, 16%) as a brown solid. 1HNMR (DMSO-d6) δ 10.56 (br s, 1H), 7.07 (d, J=12 Hz, 1H), 7.02 (m, 1H), 6.71 (d, J=8 Hz, 1H), 6.17 (s, 1H), 3.91 (br s, 2H); MS (ESI) m/e (M+H+) 150.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912199B2
Source datasetuspto-grants-2014_12
ORD IDord-60591861010e4e77b9d68b5c746e7ca8
Source noteuspto-grants-2014_12