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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188496Generated: October 29, 2026

4-Nitro-N-(tert-octyl)benzamide → 4-Amino-N-(2,4,4-trimethylpentan-2-yl)benzamide

https://huagongshe.com/reaction/2188496

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitro-N-(tert-octyl)benzamideHCID 698029—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-Amino-N-(2,4,4-trimethylpentan-2-yl)benzamideHCID 4371279976.1%

Reaction Steps

4-Nitro-N-(tert-octyl)benzamide (30 g, 0.108 mol) dissolved in 200 ml of ethyl acetate is hydrogenated for 1 hour 15 minutes at a temperature of 70-75° C. in a 500 ml hydrogenator in the presence of 4.8 g of 10% palladium-on-charcoal comprising 50% water as catalyst (hydrogen pressure: 8-10 bar). After filtering, concentrating the solvent and drying under vacuum, 20.4 g (Yield: 76%) of 4-amino-N-(tert-octyl)benzamide are obtained in the form of a pale yellow powder which is used as is in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08323624B2
Source datasetuspto-grants-2012_12
ORD IDord-534c6977fef949d19a2de618a8069a9e
Source noteuspto-grants-2012_12