HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(1-Phenyltetrazol-5-yloxy)-2,3-epoxypropane → 2-Aminotetralin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(1-Phenyltetrazol-5-yloxy)-2,3-epoxypropane | HCID 12399823 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(1-phenyltetrazol-5-yloxy)propanamine hydrochloride | HCID 14751089 | — |
| Product | 2-Aminotetralin | HCID 34677 | 100.4% |
Reaction Steps
Following the procedure of Example 27, but starting from 1-(1-phenyltetrazol-5-yloxy)-2,3-epoxypropane (4.37 g) prepared as described in BE 866,278 and 2-aminotetralin (1.48 g) in absolute ethanol (60 ml), N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(1-phenyltetrazol-5-yloxy)propanamine hydrochloride is obtained ((i): R=H, Ar=radical 60, wherein Z=Z'=H 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-76719bc6329946e595c2f6941802a886 |
| Source note | uspto-grants-1993_10 |