HuagongsheHuagongshe Chemistry Print Report · For research reference only
(E)-2-(5-chloro-2,4-dinitrophenyl)-N,N-dimethylethenamine → 5-Chloro-1H-indol-6-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (E)-2-(5-chloro-2,4-dinitrophenyl)-N,N-dimethylethenamine | HCID 59129321 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Chloro-1H-indol-6-amine | HCID 57191839 | 16.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598181B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-30914d051882463299077af7b601e9dd |
| Source note | uspto-grants-2013_12 |