HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tert-butyl-N-(4-nitrophenyl)benzamide → N-(4-aminophenyl)-4-tert-butylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tert-butyl-N-(4-nitrophenyl)benzamide | HCID 2849820 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | N-(4-aminophenyl)-4-tert-butylbenzamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05135949 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-089ce2eaaec84d91a810a69bce9f3a96 |
| Source note | uspto-grants-1992_08 |