HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178424364, compound → 2-methyl-N-[(1R)-1-phenylethyl]cyclohexan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178424364 | HCID 178424364 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-methyl-N-[(1R)-1-phenylethyl]cyclohexan-1-amine | HCID 12714217 | 80% |
Reaction Steps
A suspension of (1R,E)-N-(2-methylcyclohexylidene)-1-phenylethanamine (I-8a: 25 g, 116.27 mmol) and Raney-Ni (3.75 g) in ethanol (250 mL) was maintained under hydrogen atmosphere in a Parr hydrogenator using 5 bar pressure for 2 days. The reaction mixture was filtered and filtrate evaporated under reduced pressure. The crude compound was treated with ethereal HCl, and the precipitated salt was filtered, washed with cold ether and dried to afford 20 g (80%) of 2-methyl-N—((R)-1-phenylethyl)-cyclohexanamine (I-8b) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447039B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-350460199f344be4b1b3c00607a63c82 |
| Source note | uspto-grants-2016_09 |