Water → 5-(tert-Butyl)-2-methoxy-3-nitroaniline

HRID 2360512Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2360512
[C:1]([C:5]1[CH:6]=[C:7]([N+:16]([O-])=O)[C:8]([O:14][CH3:15])=[C:9]([N+:11]([O-:13])=[O:12])[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].O.CC1CCC=CC1>C(O)C.[Pd].C(OCC)(=O)C>[C:1]([C:5]1[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[C:8]([O:14][CH3:15])=[C:7]([NH2:16])[CH:6]=1)([CH3:4])([CH3:2])[CH3:3]

Komponenten

7

Versuchsvorschrift

2 g 5-tert-butyl-2-methoxy-1,3-dinitro-benzene are dissolved in 20 ml ethanol and combined with 2 ml of water and 100 mg of 10% palladium on charcoal. The mixture is refluxed, 1.9 ml of 4-methyl-1-cyclohexene are added and the mixture is refluxed for a further 2 hours. Then a further 1.0 ml of 4-methyl-1-cyclohexene are added dropwise and the mixture is refluxed for a further 16 hours. Then it is cooled to ambient temperature, the solvents are eliminated in vacuo and the residue is taken up in ethyl acetate. The mixture is washed with saturated aqueous sodium hydrogen carbonate solution, water, saturated aqueous sodium chloride solution and dried with sodium sulphate. The solvent is eliminated in vacuo and the product thus obtained is further reacted directly.

Aufarbeitung

  1. temperatureThe mixture is refluxed
  2. temperaturethe mixture is refluxed for a further 2 hours
  3. temperaturethe mixture is refluxed for a further 16 hours
  4. washThe mixture is washed with saturated aqueous sodium hydrogen carbonate solution, water, saturated aqueous sodium chloride solution
  5. dry with materialdried with sodium sulphate
  6. customthe product thus obtained
  7. customis further reacted directly

Quellen und Nachweise

ORD-Eintrag
ord-6834b957faa846118be0c825c6794cb0
Quelldatensatz
uspto-grants-2014_04
Patentnummer
US08686022B2

Notizen zur Reaktion

Wird geladen…