HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenamine, 4,4'-(1,4-phenylenebis(1-methylethylidene))bis(N-methyl- → HCID 54486379, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenamine, 4,4'-(1,4-phenylenebis(1-methylethylidene))bis(N-methyl- | HCID 75932 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | HCID 54486379 | HCID 54486379 | 99.8% |
Reaction Steps
100 g of α,α'-bis-(4-methylamino-phenyl)-p-diisopropylbenzene are hydrogenated in the presence of 1.0 g of the catalyst (2) (about 1% of ruthenium) at 180°- 200° C and 200° - 280° bars hydrogen pressure, until the absorption of hydrogen has ceased. Duration about 160 minutes. After cooling, the hydrogenation product is taken up in methanol, the solution is filtered and concentrated and the residue is distilled under reduced pressure. 103 g of α,α'-bis-(4-methylaminocyclohexyl)-p-diisopropylbenzene are obtained, corresponding to 100% of theory. Boiling range: 203° - 206° C/0.2 mm Hg, solidification point: 84° - 86° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04049584 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-95cc09a5a31b4d51be46fb18875e6e75 |
| Source note | uspto-grants-1977_09 |