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1,2-Dimethyl-3-nitrobenzene → 6-Methyl-2-nitrophenylpyruvic acid

HRID 52161
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 52161
[Na].[N+:2]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:6]=1[CH3:12])([O-:4])=[O:3].[C:13](OCC)(=[O:19])[C:14]([O:16]CC)=[O:15].[OH-].[Na+]>O.C(O)C>[CH3:11][C:7]1[CH:8]=[CH:9][CH:10]=[C:5]([N+:2]([O-:4])=[O:3])[C:6]=1[CH2:12][C:13](=[O:19])[C:14]([OH:16])=[O:15]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 67391,2-Dimethyl-3-nitrobenzeneHCID 7268Diethyl OxalateHCID 14798Sodium HydroxideHCID 5360545Sodium

Produkt 1

HCID 211942326-Methyl-2-nitrophenylpyruvic acidAusbeute 61 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702
Ethanol
Lösungsmittel
HCID 962WaterLösungsmittel

Versuchsvorschrift

Sodium (3.802 g, 165.38 mmol, 2.5 eq) was added portionwise into ethanol (66 mL, 1M) at 0° C. Next, 3-nitro-ortho-xylene (10.00 g, 66.15 mmol, 1 eq) and diethyl oxalate (19.33 g, 132.23 mmol, 2 eq) were added. The mixture was stirred at room temperature for 18 hours and then refluxed for 10 minutes. 1N sodium hydroxide and water were added and the reaction was stirred for one hour. The ethanol was removed under vacuum. Water was added and the aqueous solution was acidified with concentrated hydrochloric acid to ph~2. The mixture was extracted with methylene chloride. The extracts were dried (magnesium sulfate) and concentrated to give the title compound (9.0 g, 61%).

Aufarbeitung

  1. temperaturerefluxed for 10 minutes
  2. stirringthe reaction was stirred for one hour
  3. customThe ethanol was removed under vacuum
  4. additionWater was added
  5. extractionThe mixture was extracted with methylene chloride
  6. dry with materialThe extracts were dried (magnesium sulfate)
  7. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-631527924b8e4da9a6a90a47ed6c1ba9
Quelldatensatz
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05616591

Notizen zur Reaktion

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