HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Benzenamine, 3-((4-aminophenyl)methyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | (4-Chloro-3-nitrophenyl)(4-nitrophenyl)methanone | HCID 554735 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Glycol monoethyl ether | HCID 8076 | — |
| Product | Benzenamine, 3-((4-aminophenyl)methyl)- | HCID 146674 | — |
Reaction Steps
15.3 g (0.05 mol) of 3,4'-dinitro-4-chlorobenzophenone, 0.75 g of 5% Pd/C and 50 ml of ethyl cellosolve were charged in a closed glass vessel equipped with a thermometer and a stirrer. While stirring the mixture at a temperature of 75° to 80° C., hydrogen was introduced thereinto and 10.3 l (0.46 mol) of hydrogen was absorbed in 13 hours. Since no more absorption of hydrogen was observed, the reaction was terminated at this point. The reaction solution was neutralized with 3.6 g (0.06 mol) of 28% aqueous ammonia. The catalyst was removed by filtration. The filtrate was concentrated to obtain 3,4'-diaminodiphenylmethane as a brown oil. A high performance liquid chromatography revealed that the purity was 88.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04540818 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-c5bfde3dbf194434ab83be76cf615e33 |
| Source note | uspto-grants-1985_09 |