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Acetic Acid → 5-Bromo-2,3-dimethylbenzoic acid

HRID 337614
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 337614
C(O)(=O)C.[CH3:5][C:6]1[C:14]([CH3:15])=[CH:13][CH:12]=[CH:11][C:7]=1[C:8]([OH:10])=[O:9].[N+]([O-])(O)=O.[Br:20]Br>O.[N+]([O-])([O-])=O.[Ag+]>[Br:20][C:12]1[CH:13]=[C:14]([CH3:15])[C:6]([CH3:5])=[C:7]([CH:11]=1)[C:8]([OH:10])=[O:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 176Acetic AcidHCID 944Nitric AcidHCID 117822,3-Dimethylbenzoic acidHCID 24408Bromine

Produkt 1

HCID 668959895-Bromo-2,3-dimethylbenzoic acid

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 24470Silver NitrateKatalysator
HCID 962
Water
Lösungsmittel
2×

Versuchsvorschrift

To a stirred acetic acid solution (0.2 M) of 2,3-dimethylbenzoic acid (1 eq.) was added sequentially nitric acid (12 eq.), water (25 eq.) and bromine (1.1 eq.). Finally, silver nitrate (1 M aqueous solution, 1.3 eq.) was added dropwise over a period of 30 min. After another hour of stirring at RT, the crude reaction mixture was diluted with water and extracted with EtOAc. The combined organic extracts were then washed with brine, dried over Na2SO4, filtered and the filtrate concentrated in vacuo. Trituration of the crude product thus obtained in hexanes afforded the title compound as a yellow solid.

Aufarbeitung

  1. customthe crude reaction mixture
  2. extractionextracted with EtOAc
  3. washThe combined organic extracts were then washed with brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationthe filtrate concentrated in vacuo
  7. customTrituration of the crude product thus obtained in hexanes

Quellen und Nachweise

ORD-Eintrag
ord-37e33c4d6ec0494685f67ce10f914856
Quelldatensatz
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08889714B2

Notizen zur Reaktion

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