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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244466Generated: October 27, 2026

3,5-bis-(1,1-dimethylethyl)-4-hydroxy-N-[(4-nitrophenyl)methyl]-benzamide → 3,5-bis-(1,1-dimethylethyl)-4-hydroxy-N-[(4-aminophenyl)methyl]-benzamide

https://huagongshe.com/reaction/1244466

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-bis-(1,1-dimethylethyl)-4-hydroxy-N-[(4-nitrophenyl)methyl]-benzamideHCID 21918554—
ReactantHCID 178418361HCID 178418361—
SolventPalladiumHCID 23938—
SolventDichloromethane ethanolHCID 21584144—
Product3,5-bis-(1,1-dimethylethyl)-4-hydroxy-N-[(4-aminophenyl)methyl]-benzamideHCID 2191861262.1%

Reaction Steps

In a 250 ml Parr flask, 2.85 g (7.4 mmoles) of 3,5-bis-(1,1-dimethylethyl)-4-hydroxy-N-[(4-nitrophenyl)methyl]-benzamide is dissolved in 30 ml of an absolute ethanol/dichloromethane mixture (1/1) in the presence of 10% Pd/C. The mixture is agitated under 20 PSI of hydrogen, at 30° C., for one hour. After filtration on celite, the filtrate is concentrated under vacuum. The evaporation residue crystallizes spontaneously. It is left to rest overnight, the crystals are filtered out and rinsed with a mixture of diethyl ether (45 ml) and acetone (5 ml). 1.63 g (62%) of a white powder is obtained. Melting point: 188-189° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122535B2
Source datasetuspto-grants-2006_10
ORD IDord-72a14bac6fc14a68b48e4dd253a38186
Source noteuspto-grants-2006_10