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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761872Generated: October 28, 2026

2-[N-Methyl-N-(4-nitrobenzyl)amino]-5-nitroindane → 5-Amino-2-[N-(4-aminobenzyl)-N-methylamino]indane

https://huagongshe.com/reaction/1761872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[N-Methyl-N-(4-nitrobenzyl)amino]-5-nitroindaneHCID 14835246—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product5-Amino-2-[N-(4-aminobenzyl)-N-methylamino]indaneHCID 1502322358.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04829071
Source datasetuspto-grants-1989_05
ORD IDord-834771596afe4621bc1d724c54fed46e
Source noteuspto-grants-1989_05