HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sodium borohydride → (+/-)1-[Amino(phenyl)methyl]-N,N-diethylcyclopentanamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | {1-[Amino(phenyl)methyl]cyclopentyl}dimethylamine | HCID 11521393 | — |
| Edukt | 1-(Diethylamino)cyclopentanecarbonitrile | HCID 24276761 | — |
| Edukt | HCID 178506676 | HCID 178506676 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Butyl ether | HCID 8909 | — |
| Produkt | (+/-)1-[Amino(phenyl)methyl]-N,N-diethylcyclopentanamine | HCID 59347816 | 47% |
Reaktionsschritte
The title compound (0.45 g, 47%) was prepared from 1-(diethylamino)cyclopentane carbonitrile D11 (0.65 g, 3.9 mmol), and phenyllithium in dibutylether (2.4 ml of a 1.8M solution; 4.3 mmol) in THF (4 ml), followed by reaction with sodium borohydride (0.445 g, 11.7 mmol) in methanol (4 ml) in a similar manner to that described in D2. 1H NMR (CDCl3) δ: 0.42 (1H, m), 1.10 (6H, m), 1.35 (3H, m), 1.55 (1H, m), 1.66 (2H, m), 1.80-2.08 (3H, m), 2.53-2.70 (4H, m), 4.22 (1H, s), 7.20-7.31 (3H, m), 7.47 (2H, m).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07745642B2 |
| Quelldatensatz | uspto-grants-2010_06 |
| ORD ID | ord-4d59e9db98e74fe08c9c500566141da9 |
| Quellennotiz | uspto-grants-2010_06 |