HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentylamine → HCID 68143236, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentylamine | HCID 2906 | — |
| Reactant | HCID 21516834 | HCID 21516834 | — |
| Product | HCID 68143236 | HCID 68143236 | — |
Reaction Steps
Following the procedures outlined in Example 1, the 2-chloro-3,4-dibenzyloxystyrene oxide is reacted with cyclopentylamine to give 2-chloro-α-(cyclopentylaminomethyl)-3,4-dibenzyloxybenzyl alcohol hydrochloride, m.p. 181°-182°C. Similar hydrogenation over palladium-on-carbon gives 2-chloro-α-(cyclopentylaminomethyl)-3,4-dihydroxybenzyl alcohol as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03976695 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-aa8dc84a34d043a0a8cd3d8349425739 |
| Source note | uspto-grants-1976_08 |