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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908497Generated: October 28, 2026

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

https://huagongshe.com/reaction/1908497

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-2-(5-chloro-2,4-dinitrophenyl)-N,N-dimethylethenamineHCID 59129321—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product5-Chloro-1H-indol-6-amineHCID 5719183916.2%

Reaction Steps

A suspension of (E)-2-(5-chloro-2,4-dinitrophenyl)-N,N-dimethylethenamine (9.8 g, 36 mmol) and Raney Nickel (9.8 g) in EtOH (140 mL) was stirred under H2 (1 atm) at room temperature for 4 h. After filtration, the filtrate was concentrated and the residue was purified by column chromatograph (petroleum ether/ethyl acetate=10:1) to give 5-chloro-1H-indol-6-amine (0.97 g, 16%) as a gray powder. 1HNMR (CDCl3) δ 7.85 (br s, 1H), 7.52 (s, 1H), 7.03 (s, 1H), 6.79 (s, 1H), 6.34 (s, 1H), 3.91 (br s, 1H); MS (ESI) m/e (M+H+) 166.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598181B2
Source datasetuspto-grants-2013_12
ORD IDord-30914d051882463299077af7b601e9dd
Source noteuspto-grants-2013_12