HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Aminotetralin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 19788355 | HCID 19788355 | — |
| Solvent | HCID 19788274 | HCID 19788274 | — |
| Product | 2-Aminotetralin | HCID 34677 | — |
Reaction Steps
Following the procedure of Example 27, but starting from 1-acetyl-5-(2,3-epoxypropoxy)-1,2,3,4-tetrahydroquinoline (2.77 g) and 2-aminotetralin (1.49 g) in ethanol (30 ml), N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(1-acetyl-1,2,3,4-tetrahydroquinolin-5-yloxy)propanamine hydrochloride is obtained ((i): R=H, Ar=radical 66, wherein Z is methyl, and the chain is attached to position 2 of the tetralin moiety).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05254595 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-544e3145d5f84447be20b9f3f6d8b044 |
| Source note | uspto-grants-1993_10 |