Réaction #1135812

ord-45624fadc49d46e9aa387dbc6f610bda

Équation de réaction

Cc1c(O)cccc1[N+](=O)[O-]
2-methyl-3-nitrophenol
CCI
iodoethane
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCOc1cccc([N+](=O)[O-])c1C
1-ethoxy-2-methyl-3-nitrobenzene
Rendement 100.7%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewith heating
  2. 2
    Températureunder reflux for ten hours
  3. 3
    Filtrationfiltered
  4. 4
    Concentrationthe resulting filtrates were concentrated
  5. 5
    ExtractionThe resulting mixtures were extracted with ethyl acetate
  6. 6
    Lavagethe organic layers were washed with water and saturated saline
  7. 7
    Séchagewere dried over anhydrous magnesium sulfate
  8. 8
    Concentrationwere then concentrated under reduced pressure

Mode opératoire

A mixture of 2-methyl-3-nitrophenol 33.5 g, iodoethane 41 g and potassium carbonate 90 g in acetone 400 mL was stirred with heating under reflux for ten hours. The mixtures were cooled to room temperature and filtered and the resulting filtrates were concentrated. The resulting mixtures were extracted with ethyl acetate and the organic layers were washed with water and saturated saline, and were dried over anhydrous magnesium sulfate and were then concentrated under reduced pressure. The resulting residues were subjected to a silica gel column chromatography to give 1-ethoxy-2-methyl-3-nitrobenzene 39.9 g.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09380782B2uspto-grants-2016_07