HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Dodecyloxy-alpha-methylbenzylamine hydrochloride → HCID 178443274, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Dodecyloxy-alpha-methylbenzylamine hydrochloride | HCID 13012104 | — |
| Reactant | alpha-Methyl-p-phenethylbenzylamine hydrochloride | HCID 13012107 | — |
| Product | HCID 178443274 | HCID 178443274 | — |
Reaction Steps
Following essentially the same procedure described in Example 7 above and substituting p-dodecyloxy-α-methylbenzylamine hydrochloride for the α-methyl-p-phenyethylbenzylamine hydrochloride above, results in the formation of 2-(p-dodecyloxy-α-methylbenzylimino)hexahydroazepine hydrochloride having a M.P. of 186°-8° C (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04061746 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-38ac3a7b3d164440b70362beff807024 |
| Source note | uspto-grants-1977_12 |