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Dimethylamine → N,N-dimethyl-2-nitrobenzamide

HRID 2294139
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2294139
[CH3:1][NH:2][CH3:3].[OH-].[Na+].[N+:6]([C:9]1[CH:17]=[CH:16][CH:15]=[CH:14][C:10]=1[C:11](Cl)=[O:12])([O-:8])=[O:7]>O1CCOCC1>[CH3:1][N:2]([CH3:3])[C:11](=[O:12])[C:10]1[CH:14]=[CH:15][CH:16]=[CH:17][C:9]=1[N+:6]([O-:8])=[O:7]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 674DimethylamineHCID 118752-Nitrobenzoyl chlorideHCID 14798Sodium Hydroxide

Produkt 1

HCID 3261775N,N-dimethyl-2-nitrobenzamideAusbeute 57,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel2×

Versuchsvorschrift

A mixture of dimethylamine (30 g, 270 mmol) and sodium hydroxide (7.2 g, 180 mmol) in 60 mL of dioxane was stirred and 2-nitrobenzoyl chloride (23.8 mL, 180 mmol) in 100 mL of dioxane was added dropwise. The mixture was stirred at room temperature for approximately 12 hours and then partitioned between 100 mL of saturated sodium bicarbonate solution and 150 mL of ethyl acetate. The aqueous layer was extracted with ethyl acetate (2×100 mL) and the combined ethyl acetate was washed with brine, dried (Na2SO4) and concentrated. The residue was purified on silica gel by flash chromatography eluting with 4% methanol/methylene chloride to give N,N-dimethyl-2-nitrobenzamide (20 g, 103 mmol), m.p. 74°-76° C.

Aufarbeitung

  1. stirringThe mixture was stirred at room temperature for approximately 12 hours
  2. custompartitioned between 100 mL of saturated sodium bicarbonate solution and 150 mL of ethyl acetate
  3. extractionThe aqueous layer was extracted with ethyl acetate (2×100 mL)
  4. washthe combined ethyl acetate was washed with brine
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated
  7. customThe residue was purified on silica gel by flash chromatography
  8. washeluting with 4% methanol/methylene chloride

Quellen und Nachweise

ORD-Eintrag
ord-fed0dc3ce6d84218809fe4321f896155
Quelldatensatz
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05688795

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