Reaktion #88077

ord-6ddb5c05d6114e6ebc338e4750958068

Reaktionsgleichung

II
iodine
Cc1ccc(C(=O)O)cc1[N+](=O)[O-]
4-methyl-3-nitro-benzoic acid
Cc1c(I)cc(C(=O)O)cc1[N+](=O)[O-]
3-iodo-4-methyl-5-nitro-benzoic acid
Ausbeute 95.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
85°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled to room temperature
  2. 2
    workup.ADDITIONpoured over ice
  3. 3
    SonstigeThe mixture was partitioned between ethyl acetate and aqueous sodium bisulfite
  4. 4
    Sonstigethe organic layer was separated
  5. 5
    Trocknendried over MgSO4, filterd
  6. 6
    Einengenconcentrated under reduced pressure

Vorschrift

To a mixture of iodine (19.6 g, 77.3 mmol) in fuming sulfuric acid (35 mL) was added 4-methyl-3-nitro-benzoic acid (10.0 g, 55.2 mmol). The mixture was stirred at 85° C. over night, then cooled to room temperature and poured over ice. The mixture was partitioned between ethyl acetate and aqueous sodium bisulfite, and the organic layer was separated, dried over MgSO4, filterd and concentrated under reduced pressure to give 16.06 g (95%) of 3-iodo-4-methyl-5-nitro-benzoic acid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09440956B2uspto-grants-2016_09