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Hydrochloric Acid → 2,4-Dimethoxy-5-nitrobenzoic acid

HRID 2293529
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2293529
[Na].Cl[C:3]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[C:5]([O:15][CH3:16])[CH:4]=1.Cl.[CH3:18][OH:19]>>[CH3:16][O:15][C:5]1[CH:4]=[C:3]([O:19][CH3:18])[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:6]=1[C:7]([OH:9])=[O:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 5360545SodiumHCID 128487494-Chloro-2-methoxy-5-nitrobenzoic acid

Produkt 1

HCID 133076602,4-Dimethoxy-5-nitrobenzoic acid

Versuchsvorschrift

In a stream of argon, 0.30 g of metallic sodium was added to 5 ml of methanol under ice-cooling, the mixture was stirred at room temperature for a while and then 1.00 g of 4-chloro-2-methoxy-5-nitrobenzoic acid was added to the resulting solution in small portions, followed by stirring at 80° C. for 8 hours. After completion of the reaction, the reaction solution was poured into 1N hydrochloric acid aqueous solution, and the thus precipitated product of interest was collected by filtration, washed with water and then dried under a reduced pressure to give 0.80 g of 2,4-dimethoxy-5-nitrobenzoic acid.

Aufarbeitung

  1. temperaturecooling
  2. stirringby stirring at 80° C. for 8 hours
  3. customAfter completion of the reaction
  4. filtrationthe thus precipitated product of interest was collected by filtration
  5. washwashed with water
  6. customdried under a reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-3255793e0b4b46c7b2ede1e9a532758f
Quelldatensatz
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05686482

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