HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-[N-Methyl-N-(4-nitrobenzyl)amino]-5-nitroindane → 5-Amino-2-[N-(4-aminobenzyl)-N-methylamino]indane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-[N-Methyl-N-(4-nitrobenzyl)amino]-5-nitroindane | HCID 14835246 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Amino-2-[N-(4-aminobenzyl)-N-methylamino]indane | HCID 15023223 | 58.6% |
Reaction Steps
2-[N-Methyl-N-(4-nitrobenzyl)amino]-5-nitroindane (2.3 g) in ethyl acetate (60 ml) containing 5% Pd/C (. . . g) was stirred under a hydrogen atmosphere [206.8 kPa (30 psi)] for 1 hour at room temperature. The catalyst was then removed by filtration and the filtrate was evaporated to dryness in vacuo. The residue was purified by column chromatography on silica eluting with methylene chloride containing methanol (0% up to 1%). The product-containing fractions were combined and evaporated to give the title compound (1.1 g) as an oil which was used directly without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04829071 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-834771596afe4621bc1d724c54fed46e |
| Source note | uspto-grants-1989_05 |