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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846204Generated: October 31, 2026

4-tert-butyl-N-(4-nitrophenyl)benzamide → N-(4-aminophenyl)-4-tert-butylbenzamide

https://huagongshe.com/reaction/846204

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-butyl-N-(4-nitrophenyl)benzamideHCID 2849820—
CatalystPalladiumHCID 23938—
ProductN-(4-aminophenyl)-4-tert-butylbenzamideHCID 721125—

Reaction Steps

4.5 g. (0.015 mol) 4-(1,1-Dimethylethyl)-N-(4-nitrophenyl)-benzamide (Example 15 ) are hydrogenated at normal pressure and ambient temperature in the presence of 0.5 g. 10% palladium on charcoal. After 30 minutes, the reaction mixture is filtered and the filtrate is evaporated in a vacuum. The residue is digested with ligroin and filtered off with suction. There are obtained 3.4 g. (85% of theory) of the title compound; m.p. 111°-113° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05135949
Source datasetuspto-grants-1992_08
ORD IDord-089ce2eaaec84d91a810a69bce9f3a96
Source noteuspto-grants-1992_08