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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464854Generated: November 4, 2026

4-nitro-N-(2,4,4-trimethylpentan-2-yl)benzamide → 4-Amino-N-(2,4,4-trimethylpentan-2-yl)benzamide

https://huagongshe.com/reaction/1464854

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-nitro-N-(2,4,4-trimethylpentan-2-yl)benzamideHCID 698029—
ReactantHCID 178418361HCID 178418361—
CatalystWaterHCID 962—
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, in a 500 ml hydrogenator, in the presence of 4.8 g of 10% palladium-on-charcoal containing 50% of water, as catalyst (hydrogen pressure: 8-10 bar), at a temperature of 70-75° C. for 1 hour and 15 minutes. After filtration, concentration of 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 light yellow powder, which is used as it is in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999299B2
Source datasetuspto-grants-2015_04
ORD IDord-b2bfde9ed2a34503855b977f3d67f798
Source noteuspto-grants-2015_04