HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitro-N-(tert-octyl)benzamide → 4-Amino-N-(2,4,4-trimethylpentan-2-yl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitro-N-(tert-octyl)benzamide | HCID 698029 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Amino-N-(2,4,4-trimethylpentan-2-yl)benzamide | HCID 43712799 | 76.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08323624B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-534c6977fef949d19a2de618a8069a9e |
| Source note | uspto-grants-2012_12 |