Réaction #2161253

ord-b793f13c47284608a67f50fde8aaafc1

Équation de réaction

C1CCCCC1.CCOC(C)=O
cyclohexane ethyl acetate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CI
iodomethane
CCOC(=O)c1nc([N+](=O)[O-])c[nH]1
ethyl 4-nitro-1H-imidazole-2-carboxylate
CCOC(=O)c1nc([N+](=O)[O-])cn1C
Ethyl 1-methyl-4-nitro-1H-imidazole-2-carboxylate

Solvants

Conditions de réaction

Température
60°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureAfter cooling
  2. 2
    Filtrationthe mixture is filtered
  3. 3
    Lavagethe residue is washed with dichloromethane
  4. 4
    AutreThe solid obtained
  5. 5
    Autreis dried in vacuo

Mode opératoire

6.80 g (36.7 mmol) of ethyl 4-nitro-1H-imidazole-2-carboxylate are dissolved in 140 ml of acetone, and 11.2 g (80.8 mmol) of potassium carbonate and 4.57 ml (73.5 mmol) of iodomethane are added. The mixture is then stirred at 60° C. for 4 h. According to TLC (cyclohexane/ethyl acetate 2:1), the starting material has been converted completely. After cooling, the mixture is filtered, the residue is washed with dichloromethane and the filtrate is freed from the solvent. The solid obtained is dried in vacuo.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07919489B2uspto-grants-2011_04