Reaktion #3199

ord-62f911c33ec34c2dbe633593e1d5ee82

Reaktionsgleichung

O=C1Nc2cc(Cl)cc(Cl)c2C1=O
4,6-dichloro-1H-indole-2,3-dione
CC(=O)O
acetic acid
O=c1[nH]c2cc(Cl)cc(Cl)c2c(=O)o1
title compound
Ausbeute 72.0%
O=c1[nH]c2cc(Cl)cc(Cl)c2c(=O)o1
5,7-Dichloro-2H-3,1-benzoxazine-2,4(1H)-dione
Ausbeute 72.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    Filtrationfiltered
  3. 3
    Sonstigeto separate the precipitated solids
  4. 4
    WaschenThe solids were washed thoroughly with water
  5. 5
    Sonstigedried

Vorschrift

To a stirred solution of 4,6-dichloro-1H-indole-2,3-dione (5.00 g, 23.2 mM) in acetic acid (21 mL) and acetic anhydride (21 mL) at 80° C. was added in small portions chromium trioxide (4.12 g, 41.3 mM). The temperature of the reaction mixture was maintained between 80°-90° C. during the addition of the chromium trioxide. After the addition was complete, the reaction mixture was diluted with water (100 mL) and then filtered to separate the precipitated solids. The solids were washed thoroughly with water and then dried to obtain the title compound as a yellow solid (4.13 g, 72%); MS(CI): 232 (M+H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05733910uspto-grants-1998_03