Reaktion #170138

ord-8db0c46b33d045a3bf08d5ac027168f0

Reaktionsgleichung

CCOC(=O)/N=N/C(=O)OCC
DEAD
OC1CN(C(c2ccccc2)c2ccccc2)C1
N-benzhydrylazetidin-3-ol
O=C1c2ccccc2C(=O)N1O
N-hydroxyphthalimide
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
O=C1c2ccccc2C(=O)N1OC1CN(C(c2ccccc2)c2ccccc2)C1
title compound
Ausbeute 37.3%
O=C1c2ccccc2C(=O)N1OC1CN(C(c2ccccc2)c2ccccc2)C1
2-{[1-(Diphenylmethyl)azetidin-3-yl]oxy}-1H-isoindole-1,3(2H)-dione
Ausbeute 37.3%

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto warm to room temperature
  2. 2
    EinengenThe reaction mixture was concentrated
  3. 3
    SonstigeThe residue was purified on column chromatography (eluent: pentane/EtOAc 7/3 to 4/6)

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08846711B2uspto-grants-2014_09