HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Aminotetralin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 19788318 | HCID 19788318 | — |
| Solvent | HCID 14751007 | HCID 14751007 | — |
| Product | 2-Aminotetralin | HCID 34677 | — |
Reaction Steps
Following the procedure of Example 27, but starting from 4-(4-ethoxycarbonyl-1,2,3-thiadiazol-5-yl)-1-(2,3-epoxypropoxy)benzene (2.94 g) and 2-aminotetralin (1.49 g) in absolute ethanol (20 ml), N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-[4-(4-ethoxycarbonyl-1,2,3-thiadiazol-5-yl)phenoxy]propanamine hydrochloride is obtained ((i): R=H, Ar=radical 63, wherein Z is a 4-COOC2H5 group, 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-414322dbf5984641a2ea827c63aeafa2 |
| Source note | uspto-grants-1993_10 |