HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → HCID 20552833, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | HCID 22987706 | HCID 22987706 | — |
| Product | HCID 20552833 | HCID 20552833 | — |
Reaction Steps
A secondary N-benzylamine can likewise be debenzylated to produce the desired primary amine. To prepare such a secondary benzlamine, 3-chloro-1-(o-anisyloxy)propylbenzene or other 1-substituted phenyl-3-chloropropylbenzene, utilized as an intermediate in an earlier procedure, can be reacted with benzylamine to yield N-benzyl 3-phenyl-3-(o-anisyloxy)propylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04313896 |
| Source dataset | uspto-grants-1982_02 |
| ORD ID | ord-d2712516f07743eb8c160545f1ea9b5c |
| Source note | uspto-grants-1982_02 |