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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2172012Erstellt: 24. Oktober 2026

N-Hydroxyphthalimide → 2-{[1-(Diphenylmethyl)azetidin-3-yl]oxy}-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/de/reaction/2172012

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-HydroxyphthalimideHCID 10665—
EduktTriphenylphosphineHCID 11776—
Edukt1-(Diphenylmethyl)azetidin-3-olHCID 330448—
EduktDiethyl azodicarboxylateHCID 5462977—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-{[1-(Diphenylmethyl)azetidin-3-yl]oxy}-1H-isoindole-1,3(2H)-dioneHCID 6833802437,3%

Reaktionsbedingungen

Temperatur0 °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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09051321B2
Quelldatensatzuspto-grants-2015_06
ORD IDord-d0a31ed623b44b9582b5a1c6d06ff3fe
Quellennotizuspto-grants-2015_06