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2,3-Dinitrophenol → 1-Methoxy-2,3-dinitrobenzene

HRID 221518
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 221518
[N+:1]([C:4]1[C:9]([N+:10]([O-:12])=[O:11])=[CH:8][CH:7]=[CH:6][C:5]=1[OH:13])([O-:3])=[O:2].IC.[C:16]([O-])([O-])=O.[K+].[K+]>>[N+:1]([C:4]1[C:9]([N+:10]([O-:12])=[O:11])=[CH:8][CH:7]=[CH:6][C:5]=1[O:13][CH3:16])([O-:3])=[O:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 61912,3-DinitrophenolHCID 6328Methyl iodideHCID 11430Potassium Carbonate

Produkt 1

HCID 2428251-Methoxy-2,3-dinitrobenzeneAusbeute 100 %

Versuchsvorschrift

A mixture of 2,3-dinitrophenol (5.43 mmol, 1 g), iodomethane (21.7 mmol, 1.35 mL) and K2CO3 (21.7 mmol, 2.99 g) was stirred at room temperature for 14 h. The reaction was then filtered through celite and the filter bed was washed with additional acetone. The filtrate was concentrated to provide 2,3-dinitroanisole (100%), which was dissolved in a mixture of EtOH/H2O (1:1, 20 mL) and Fe (19.4 mmol, 1.06 g) and concentrated HCl (8 drops) was added. The mixture was refluxed for 90 min., after which it was filtered through celite and the filter bed was washed with additional EtOH. The filtrate was concentrated and basified (pH>12) with 4 M NaOH and the aqueous layer was extracted with CH2Cl2. The organic phase was then separated and washed with brine, dried MgSO4 and concentrated to provide 2,3-diaminoanisole 36b (0.65 g).

Aufarbeitung

  1. filtrationThe reaction was then filtered through celite
  2. washthe filter bed was washed with additional acetone
  3. concentrationThe filtrate was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-c09bce2eeafa489c83187f3b7a592430
Quelldatensatz
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08207173B2

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