N-bromobutanimide → 3-Amino-4-bromo-2,6-dichlorobenzoic acid

HRID 2201771Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2201771
[NH2:1][C:2]1[C:3]([Cl:12])=[C:4]([C:8]([Cl:11])=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].[Br:13]N1C(=O)CCC1=O>C(#N)C>[NH2:1][C:2]1[C:3]([Cl:12])=[C:4]([C:8]([Cl:11])=[CH:9][C:10]=1[Br:13])[C:5]([OH:7])=[O:6]

Komponenten

4

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

A mixture of 3-amino-2,6-dichlorobenzoic acid (5 g, 24 mmol, Step b) in acetonitrile (50 mL) was treated with N-bromosuccinimide (5.1 g, 29 mmol) and the reaction mixture was stirred at 90° C. for 45 minutes. Acetonitrile was removed in vaccuo and the residue was partitioned between water (200 mL) and ethyl acetate (200 mL). The organic layer was separated and the aqueous layer was again extracted with ethyl acetate (2×100 mL). The combined organics were dried over anhydrous sodium sulfate and concentrated to afford 3-amino-4-bromo-2,6-dichloro-benzoic acid (5 g, 73%).

Aufarbeitung

  1. customAcetonitrile was removed in vaccuo
  2. customthe residue was partitioned between water (200 mL) and ethyl acetate (200 mL)
  3. customThe organic layer was separated
  4. extractionthe aqueous layer was again extracted with ethyl acetate (2×100 mL)
  5. dry with materialThe combined organics were dried over anhydrous sodium sulfate
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-6d591217143646f0b31c819ba6b74714
Quelldatensatz
uspto-grants-2016_06
Patentnummer
US09364466B2

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