HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
N-Hydroxyphthalimide → 2-{[1-(Diphenylmethyl)azetidin-3-yl]oxy}-1H-isoindole-1,3(2H)-dione
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | N-Hydroxyphthalimide | HCID 10665 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | 1-(Diphenylmethyl)azetidin-3-ol | HCID 330448 | — |
| Edukt | Diethyl azodicarboxylate | HCID 5462977 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-{[1-(Diphenylmethyl)azetidin-3-yl]oxy}-1H-isoindole-1,3(2H)-dione | HCID 68338024 | 37,3% |
Reaktionsbedingungen
| Temperatur | 0 °C |
|---|
Reaktionsschritte
To a solution of N-benzhydrylazetidin-3-ol (1.0 g, 4.18 mmol) in anhydrous THF (66 mL) under nitrogen were added N-hydroxyphthalimide (750 mg, 4.60 mmol) and triphenylphosphine (2.19 g, 8.36 mmol). The reaction mixture was cooled to 0° C. and DEAD (1.52 mL, 8.36 mmol) was added dropwise. The solution was allowed to warm to room temperature and stirred overnight. The reaction mixture was concentrated under reduced. The residue was purified on column chromatography (eluent: pentane/EtOAc 7/3 to 4/6) to give the title compound (600 mg, 37%) as a wax.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09051321B2 |
| Quelldatensatz | uspto-grants-2015_06 |
| ORD ID | ord-d0a31ed623b44b9582b5a1c6d06ff3fe |
| Quellennotiz | uspto-grants-2015_06 |