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

HRID 2201809Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2201809
[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-dichloro-benzoic 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 under vacuum and the residue was partitioned between water (200 mL) and ethyl acetate (200 mL). Organic layer was separated and the aqueous layer was again extracted with ethyl acetate (2×100 mL). The combined organic layer was dried over anhydrous sodium sulphate and concentrated to yield 3-amino-4-bromo-2,6-dichloro-benzoic acid (5 g, 73%).

Aufarbeitung

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

Quellen und Nachweise

ORD-Eintrag
ord-2ff9645daf2d40f69893aa5e0f929871
Quelldatensatz
uspto-grants-2016_06
Patentnummer
US09364466B2

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