Reaktion #46056

ord-9640bdcdf36c4971b8fd9af98d635629

Reaktionsgleichung

Clc1ccc2[nH]nnc2c1
5-Chloro-1H-benzotriazole
O=[N+]([O-])O
Nitric acid
O=[N+]([O-])c1c(Cl)ccc2[nH]nnc12
[ 22 ]
Ausbeute 83.0%
O=[N+]([O-])c1c(Cl)ccc2[nH]nnc12
4-Nitro-5-chloro-1H-benzotriazole
Ausbeute 83.0%

Lösungsmittel

Reaktionsbedingungen

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

Aufarbeitung

  1. 1
    workup.WAITat 60° C. for an additional 1 hour
  2. 2
    TemperaturThe solution was cooled to room temperature
  3. 3
    workup.ADDITIONpoured over ice
  4. 4
    Sonstigeto precipitate a white solid
  5. 5
    FiltrationThe solid was collected by filtration
  6. 6
    Waschenwashed with copious amounts of water until neutral

Vorschrift

5-Chloro-1H-benzotriazole (3.08 g, 20 mmol) was dissolved in conc. sulphuric acid (40 ml) and cooled to 0° C. on an ice bath. Nitric acid (40 ml, excess) was added drop wise to the cooled solution over a period of 20 minutes. Stirring was continued for 1 hour at 0° C. and then at 60° C. for an additional 1 hour, by which time TLC (A) indicated the conversion of starting material. The solution was cooled to room temperature and poured over ice to precipitate a white solid. The solid was collected by filtration and washed with copious amounts of water until neutral to afford [22] in 83% yield. Rf (A) 0.49 δH(400 MHz; DMSO-d6) 7.75 (1H, d, J8.8, BT) 8.38 (1H, br s, BT); m/z (EI−HR) 197.99383 [(M) calc. for C6H3N4O235Cl 197.99445] and 199.99345 [(M) calc. for C6H3N4O237Cl 199.99150].

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07741102B2uspto-grants-2010_06