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Nitric Acid → Methyl 4-nitro-3-valerylaminobenzoate

HRID 1655459
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1655459
[C:1]([NH:7][C:8]1[CH:9]=[C:10]([CH:15]=[CH:16][CH:17]=1)[C:11]([O:13][CH3:14])=[O:12])(=[O:6])[CH2:2][CH2:3][CH2:4][CH3:5].[N+:18]([O-])([OH:20])=[O:19]>C(OC(=O)C)(=O)C.S(=O)(=O)(O)O>[N+:18]([C:17]1[CH:16]=[CH:15][C:10]([C:11]([O:13][CH3:14])=[O:12])=[CH:9][C:8]=1[NH:7][C:1](=[O:6])[CH2:2][CH2:3][CH2:4][CH3:5])([O-:20])=[O:19]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 944Nitric AcidHCID 19171455Methyl 3-pentanamidobenzoate

Produkt 1

HCID 19792184Methyl 4-nitro-3-valerylaminobenzoateAusbeute 36 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1118Sulfuric AcidKatalysatorHCID 7918Acetic AnhydrideLösungsmittel

Versuchsvorschrift

To a solution of methyl 3-valerylaminobenzoate (2.3 g) in acetic anhydride (12 ml) was added dropwise fuming nitric acid (1.4 ml) while stirring under ice-cooling. To the mixture was added one drop of conc. sulfuric acid and the mixture was stirred for two hours. To the reaction mixture was added ice-water and it was extracted with ethyl acetate. The organic layer was washed with an aqueous solution of sodium bicarbonate and water and then dried. The solvent was evaporated to dryness, and the residue was purified by column chromatography on silica gel to afford a brown oil (1.0 g, 36%).

Aufarbeitung

  1. temperaturecooling
  2. stirringthe mixture was stirred for two hours
  3. extractionwas extracted with ethyl acetate
  4. washThe organic layer was washed with an aqueous solution of sodium bicarbonate and water
  5. customdried
  6. customThe solvent was evaporated to dryness
  7. customthe residue was purified by column chromatography on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-145902ef52d14e1fb265a43d938ed10f
Quelldatensatz
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05250554

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