HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-nitro-N-(2,4,4-trimethylpentan-2-yl)benzamide → 4-Amino-N-(2,4,4-trimethylpentan-2-yl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-nitro-N-(2,4,4-trimethylpentan-2-yl)benzamide | HCID 698029 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Water | HCID 962 | — |
| 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, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08999299B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-b2bfde9ed2a34503855b977f3d67f798 |
| Source note | uspto-grants-2015_04 |