Reacción #65632

ord-8e88240b57da42d69ecdb18994186b06

Ecuación de reacción

Clc1ccc2c(c1)N=Cc1ccccc1O2
8-chloro-dibenz[b,f]-[1,4]oxazepine
O=C1OC(=O)c2ccccc21
phthalic anhydride
O=C(O)c1ccccc1C(=O)N1Cc2ccccc2Oc2ccc(Cl)cc21
title compound
Rendimiento 70.3%
O=C(O)c1ccccc1C(=O)N1Cc2ccccc2Oc2ccc(Cl)cc21
2-[(8-chlorodibenz[b,f][1,4]oxazepin-10(11H)-yl)carbonyl]benzoic acid
Rendimiento 70.3%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas heated
  2. 2
    Temperaturato reflux for 4 days
  3. 3
    ConcentraciónThe mixture was concentrated
  4. 4
    Otrothe residue was triturated with ether
  5. 5
    FiltraciónThe precipitated solid was filtered

Procedimiento

A stirred mixture of 8-chloro-dibenz[b,f]-[1,4]oxazepine (3.35 g) and phthalic anhydride (2.13 g) in THF (40 mL) was heated to reflux for 4 days. The mixture was concentrated and the residue was triturated with ether. The precipitated solid was filtered to give the title compound as a white solid (3.84 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05420270uspto-grants-1995_05