HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
p-Toluenesulfonic acid → Pyrrolidine, 1-(6-chloro-3,4-dihydro-2-naphthalenyl)-
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | Pyrrolidine | HCID 31268 | — |
| Edukt | 6-Chloro-2-tetralone | HCID 4456139 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | Pyrrolidine, 1-(6-chloro-3,4-dihydro-2-naphthalenyl)- | HCID 10444008 | — |
Reaktionsschritte
1155 g (6.4 mol) of 6-chloro-3,4-dihydro-2(1H)-naphthalenone were dissolved in 5 l of toluene, 500 g (7.0 mol) of pyrrolidine and subsequently a solution of 26 g (0.14 mol) of p-toluenesulphonic acid in toluene were added dropwise thereto and the mixture was boiled under reflux. When about 120 ml of water had separated, 4 l of toluene were distilled off and the mixture was left to cool slowly. A solid crystallized out. Filtration and washing with acetone gave 1-(6-chloro-3,4-dihydro-2-naphthyl)pyrrolidine of melting point 117°-118°. Concentration of the mother liquor, suspension of the residue in ether, filtration and washing with acetone gave a further portion of the above product of melting point 117°-118°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04749791 |
| Quelldatensatz | uspto-grants-1988_06 |
| ORD ID | ord-9f02db5146114d8b94e41f4ce3ed4995 |
| Quellennotiz | uspto-grants-1988_06 |