HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Tetrahydrofuran → 4-(5-Methyl-2-phenyl4-oxazolylmethoxy)benzyloxyamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Edukt | N-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]phthalimide | HCID 22344648 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Potassium Carbonate | HCID 11430 | — |
| Produkt | 4-(5-Methyl-2-phenyl4-oxazolylmethoxy)benzyloxyamine | HCID 22344593 | 90,3% |
Reaktionsschritte
Hydrazine monohydrate (1.15 ml) was added to a solution of N-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]phthalimide (5.22 g) in ethanol (40 ml)-tetrahydrofuran (40 ml) and heated under reflux for 3 hours. The reaction mixture was cooled to room temperature, diluted with an aqueous solution of potassium carbonate and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The remaining crystals were recrystallized from ethyl acetate-hexane to obtain 4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamine (3.32 g, yield 90%) as colorless crystals. m.p. 68-69° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06924300B2 |
| Quelldatensatz | uspto-grants-2005_08 |
| ORD ID | ord-1e6ff1e8dd1647bd82d1a191a0ea3815 |
| Quellennotiz | uspto-grants-2005_08 |