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Water → 5-Bromo-3-chloro-2-hydroxy-4-methoxybenzoic acid

HRID 629381
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 629381
[Cl:1][C:2]1[C:3]([OH:13])=[C:4]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[C:5]([OH:7])=[O:6].[Br:14]Br.O>C(O)(=O)C>[Br:14][C:9]1[C:10]([O:11][CH3:12])=[C:2]([Cl:1])[C:3]([OH:13])=[C:4]([CH:8]=1)[C:5]([OH:7])=[O:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 962WaterHCID 24408BromineHCID 847769843-Chloro-2-hydroxy-4-methoxybenzoic acid

Produkt 1

HCID 1184681135-Bromo-3-chloro-2-hydroxy-4-methoxybenzoic acidAusbeute 67,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

To a solution of 3-chloro-2-hydroxy-4-methoxybenzoic acid (11.1 g) in acetic acid (275 mL) was added bromine (8.79 g) at room temperature, and the mixture was stirred for 16 hr. To the reaction mixture was added water, and the precipitate was collected by filtration. The precipitate was washed with water, and dissolved in ethyl acetate, and the solution was washed with water and saturated brine. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (10.4 g).

Aufarbeitung

  1. filtrationthe precipitate was collected by filtration
  2. washThe precipitate was washed with water
  3. dissolutiondissolved in ethyl acetate
  4. washthe solution was washed with water and saturated brine
  5. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  6. customthe solvent was evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-c0169a4f5e5149f38c2f2c304e110a3b
Quelldatensatz
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09315458B2

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