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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654196Generated: October 29, 2026

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

https://huagongshe.com/reaction/654196

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 numberUS05130334
Source datasetuspto-grants-1992_07
ORD IDord-32b3f70788a84cc09720243b5cc3c4b6
Source noteuspto-grants-1992_07