HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 21434879, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | 2-Methyl-2-nitro-1-phenylpropane | HCID 3080778 | — |
| Reactant | HCID 54491284 | HCID 54491284 | — |
| Catalyst | Ruthenium | HCID 23950 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 21434879 | HCID 21434879 | 84.3% |
Reaction Steps
Four grams of 2[ 4-nitrophenyl]-2-[4-(2-nitro-2-methylpropyl)phenyl]propane, prepared from the condensation reaction of nitrobenzene and 1,1-dimethyl-1-nitro-2-phenylethane with acetone, dissolved in 50 ml of dioxane, was hydrogenated at 150° C. and 1400 p.s.i.g. for 5 hours in the presence of 0.55 gram of 10% ruthenium on carbon. The reaction mixture was filtered, and the filtrate was fractionally distilled to produce 2.9 grams of 2[4-aminocyclohexyl]-2-[4-(2-amino-2-methylpropyl)cyclohexyl]propane (boiling point 98° C. at 0.55 mm Hg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024185 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-9b40c78a035448b3b0a9d46a468eb948 |
| Source note | uspto-grants-1977_05 |