HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sodium hydride → 7-[(2-Piperidinoethoxy)methyl]-2-phenylbenzofuran hydrochloride
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Piperidine, 1-(2-chloroethyl)-, hydrochloride | HCID 74826 | — |
| Edukt | 7-Hydroxymethyl-2-phenylbenzofuran | HCID 14514949 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 7-[(2-Piperidinoethoxy)methyl]-2-phenylbenzofuran hydrochloride | HCID 19840313 | 51% |
Reaktionsschritte
7-Hydroxymethyl-2-phenylbenzofuran (1.57 g) is dissolved in dimethylsulfoxide (10 ml), and sodium hydride (60% oil dispersion) (0.57 g) is added thereto. After the mixture is stirred for 10 minutes, N-(2-chloroethyl)piperidine hydrochloride (1.35 g) is added to the mixture and the mixture is stirred at room temperature for 4 hours. The mixture is diluted with water and extracted with ethyl acetate. The extract is washed with water, dried and concentrated under reduced pressure to remove solvent. The residue is converted to its hydrochloride and recrystallized from ethyl acetate, whereby 7-[(2-piperidinoethoxy)methyl]-2-phenylbenzofuran hydrochloride (1.32 g) is obtained. Yield: 51%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04882340 |
| Quelldatensatz | uspto-grants-1989_11 |
| ORD ID | ord-c84902389f744f2fad958c64feb3dde5 |
| Quellennotiz | uspto-grants-1989_11 |