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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73942Generated: October 26, 2026

[2-(5-Fluoro-2,4-dinitro-phenyl)-vinyl]-dimethyl-amine → 5-Fluoro-1H-indol-6-amine

https://huagongshe.com/reaction/73942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[2-(5-Fluoro-2,4-dinitro-phenyl)-vinyl]-dimethyl-amineHCID 57060726—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product5-Fluoro-1H-indol-6-amineHCID 1502233621.2%

Reaction Steps

A suspension of [2-(5-fluoro-2,4-dinitro-phenyl)-vinyl]-dimethyl-amine (8 g, 31.4 mmol) and Raney Ni (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 chromatography (Pet.Ether/EtOAc=5/1) to give 5-fluoro-1H-indol-6-ylamine (B-20) as a brown solid (1 g, 16%). 1H NMR (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); ESI-MS 150.1 m/z (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829204B2
Source datasetuspto-grants-2014_09
ORD IDord-6b0b8ef0aee64427acd7cf19b0ba09f5
Source noteuspto-grants-2014_09