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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921286Generated: October 25, 2026

N-(4-methyl-3-nitrophenyl)cyclopropanecarboxamide → N-(3-amino-4-methylphenyl)cyclopropanecarboxamide

https://huagongshe.com/reaction/1921286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-methyl-3-nitrophenyl)cyclopropanecarboxamideHCID 4104437—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-(3-amino-4-methylphenyl)cyclopropanecarboxamideHCID 2469353794.8%

Reaction Steps

N-(4-Methyl-3-nitrophenyl)cyclopropanecarboxamide (409 mg) was hydrogenated over 10% Pd/C (50% wet, 80 mg) at atmospheric pressure of hydrogen in MeOH (20 mL) for 5 hr. The catalyst was removed by filtration through Celite® pad and the filtrate was evaporated in vacuo to give N-(3-amino-4-methylphenyl)cyclopropanecarboxamide (335 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173684B2
Source datasetuspto-grants-2012_05
ORD IDord-1148f2f8c34e49a9a37dc682729e6a91
Source noteuspto-grants-2012_05