HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Methyl-p-phenethylbenzylamine hydrochloride → HCID 178463291, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Methyl-p-phenethylbenzylamine hydrochloride | HCID 13012107 | — |
| Reactant | HCID 13012111 | HCID 13012111 | — |
| Product | HCID 178463291 | HCID 178463291 | — |
Reaction Steps
Following essentially the same procedure described in Example IV above and substituting ρ-(fluoren-9-ylidenemethyl)-α-methylbenzylamine hydrochloride for the α-methyl-ρ-phenethylbenzylamine hydrochloride above results in the formation of 2-[[1-[ρ-(fluoren-9-ylidenemethyl)phenyl]ethylimino]]-hexahydro-1H-azepine, having a M.P. of 265.5°-7.5° C. (dec.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04055561 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-ff7f7a8bc76d470daaec03bd593487dc |
| Source note | uspto-grants-1977_10 |