HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Nitropropane → HCID 178457349, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Nitropropane | HCID 398 | — |
| Reactant | 4-Nitrobenzyl chloride | HCID 7482 | — |
| Reactant | Lithium hydride | HCID 62714 | — |
| Reactant | 1-(2-Methyl-2-nitropropyl)-4-nitrobenzene | HCID 228091 | — |
| Catalyst | Ruthenium | HCID 23950 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178457349 | HCID 178457349 | — |
| Product | HCID 178457350 | HCID 178457350 | — |
Reaction Steps
Ten grams of 2-(4-nitrophenyl)-1,1-dimethyl-1-nitroethane, prepared from the reaction of p-nitrobenzyl chloride and 2-nitropropane catalyzed by lithium hydride, dissolved in dioxane, was hydrogenated in the presence of 0.8 grams of 10% ruthenium on carbon at 120° C. and 1600 p.s.i.g. for 7 hours. The reaction mixture was filtered and the filtrate was fractionally distilled to produce 6.7 grams of trans 2-(4-aminocyclohexyl)-1,1-dimethylethylamine (A) boiling point 78° C. at 0.2 mm Hg, and 1.5 grams of cis 2-(4-aminocyclohexyl)-1,1-dimethylethylamine (B), boiling point 69° C. at 0.2 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024185 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-f7689466884c423d86f787d6c5c21487 |
| Source note | uspto-grants-1977_05 |