Water → 2-(5-Methoxy-4-methyl-2-nitrophenyl)acetonitrile

HRID 1258198Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1258198
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N+:9]([O-:11])=[O:10])=[CH:5][C:4]=1[CH3:12].ClC1C=CC(O[CH2:19][C:20]#[N:21])=CC=1.CC(C)([O-])C.[K+].O>CN(C)C=O>[CH3:1][O:2][C:3]1[C:4]([CH3:12])=[CH:5][C:6]([N+:9]([O-:11])=[O:10])=[C:7]([CH2:19][C:20]#[N:21])[CH:8]=1

Komponenten

6

Edukt 4

HCID 962WaterHCID 3064442-(4-Chlorophenoxy)acetonitrileHCID 6435201-Methoxy-2-methyl-4-nitrobenzeneHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 216711082-(5-Methoxy-4-methyl-2-nitrophenyl)acetonitrileAusbeute 40,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To a solution of 1-methoxy-2-methyl-4-nitrobenzene (0.4 g) and (4-chlorophenoxy)acetonitrile (0.4 g) in N,N-dimethylformamide (10 mL) was added potassium tert-butoxide (0.3 g) under ice cooling and this mixture was stirred at the same temperature for 1 hours. This mixture was poured into water and the resulting mixture was extracted with ethyl acetate. This organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate) to give the title compound (0.2 g).

Aufarbeitung

  1. extractionthe resulting mixture was extracted with ethyl acetate
  2. washThis organic layer was washed with water and brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe solvent was removed under reduced pressure
  5. customThe residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-1b7514515f414996ba0bd10d66ef7517
Quelldatensatz
uspto-grants-2013_06
Patentnummer
US08466152B2

Notizen zur Reaktion

Wird geladen…