HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Cyclohexyl-alpha-methylbenzylamine hydrochloride → 2-(rho-Cyclohexyl-alpha-methylbenzylimino)hexahydroazepine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Cyclohexyl-alpha-methylbenzylamine hydrochloride | HCID 13012105 | — |
| Reactant | alpha-Methyl-p-phenethylbenzylamine hydrochloride | HCID 13012107 | — |
| Product | 2-(rho-Cyclohexyl-alpha-methylbenzylimino)hexahydroazepine hydrochloride | HCID 178463289 | — |
Reaction Steps
Following essentially the same procedure described in Example 7 above and substituting p-cyclohexyl-α-methylbenzylamine hydrochloride for the α-methyl-p-phenyethylbenzylamine hydrochloride above, results in the formation of 2-(p-cyclohexyl-α-methylbenzylimino)-hexahydroazepine hydrochloride having a M.P. of 245°-7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04061746 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-03edca94a5584c77bf1df3d621f42a11 |
| Source note | uspto-grants-1977_12 |