HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 4-tert-Butylcyclohexylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4-tert-Butylcyclohexanone | HCID 7392 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | 4-tert-Butylcyclohexylamine | HCID 79396 | — |
Reaction Steps
312 g of 4-tert-butylcyclohexanone in 500 ml of ammonia-saturated methanol were hydrogenated at 100° C. and 100 bar in the presence of 10 g of Raney nickel. The catalyst was filtered off, the mixture was concentrated, and the crude product was purified on a thin-layer evaporator (105°/0.5 mm). 303 g of colorless liquid were obtained. The product is an isomer mixture in which the cis-cyclohexylamine derivative prevails. ##STR11##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05571815 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-51b6a337690d4903814639a2d72328e2 |
| Source note | uspto-grants-1996_11 |