HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethyl-4-nitrobenzylamine → Benzenemethanamine, 4-amino-N,N-dimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethyl-4-nitrobenzylamine | HCID 278498 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Benzenemethanamine, 4-amino-N,N-dimethyl- | HCID 308051 | — |
Reaction Steps
In a 30 l autoclave was placed a suspension in which 10 g. of a palladium-carbon catalyst was suspended in 50 ml of ethanol, and 890 g. of N,N-dimethyl-p-nitrobenzylamine and 10 l of ethanol were charged thereinto. Then, hydrogenation was carried out at 35° C. under 30 atm., and when the consumption of hydrogen was ceased, the reaction mixture was taken out of the autoclave. After the palladium-carbon was removed by filtration and the ethanol was removed by distillation to concentrate the filtrate, the resulting residue was distilled under reduced pressure to give a light-yellow liquid which was the desired product boiling at 105° to 108° C./2 mmHg. Yield: 675 g. (90%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04193800 |
| Source dataset | uspto-grants-1980_03 |
| ORD ID | ord-7b2a8f00b9f1488bbf5aef3da4148e3c |
| Source note | uspto-grants-1980_03 |