HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-[[4-(4,5,6,7-tetrahydrobenzofuran-2-yl)]phenoxy]propanamine hydrochloride → 2-Aminotetralin
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-[[4-(4,5,6,7-tetrahydrobenzofuran-2-yl)]phenoxy]propanamine hydrochloride | HCID 14750973 | — |
| Edukt | 4-(4,5,6,7-Tetrahydrobenzofuran-2-yl)-1-(2,3-epoxypropoxy)benzene | HCID 19788258 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2-Aminotetralin | HCID 34677 | — |
Reaktionsschritte
Following the procedure of Example 27, but starting from 4-(4,5,6,7-tetrahydrobenzofuran-2-yl)-1-(2,3-epoxypropoxy)benzene (27 g), obtained according to the teaching of U.S. Pat. No. 3,894,058, and 2-aminotetralin (14.85 g) in ethanol (150 ml), N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-[[4-(4,5,6,7-tetrahydrobenzofuran-2-yl)]phenoxy]propanamine hydrochloride is obtained ((i): R=H, Ar=radical 31 wherein Z is H, and the chain is attached to position 2 of the tetralin moiety).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05254595 |
| Quelldatensatz | uspto-grants-1993_10 |
| ORD ID | ord-a4de43d371ff4ef69ee30b853ce9adfb |
| Quellennotiz | uspto-grants-1993_10 |