Sodium Hydroxide → 4-bromo-1,3-dimethyl-1H-pyrazole-5-carboxylic acid

HRID 244666

Reaktionsgleichung

Reaktionsgleichung von HRID 244666
[Br:1][C:2]1[C:3]([CH3:13])=[N:4][N:5]([CH3:12])[C:6]=1[C:7]([O:9]CC)=[O:8].[OH-].[Na+]>CO>[Br:1][C:2]1[C:3]([CH3:13])=[N:4][N:5]([CH3:12])[C:6]=1[C:7]([OH:9])=[O:8]

Komponenten

4

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

To a solution of ethyl 4-bromo-1,3-dimethyl-1H-pyrazole-5-carboxylate (200 mg) (for example, available from Sinova) in methanol (10 ml) was added 2M sodium hydroxide (5 ml) and the mixture stirred at 20° C. for 18 h. The mixture was concentrated in vacuo and the residue taken up in water (10 ml) and acidified to pH=5 using 2M hydrochloric acid. The mixture was extracted with ethyl acetate (20 ml) dried over sodium sulphate and evaporated to give the title compound (25 mg) as a white solid.

Aufarbeitung

  1. concentrationThe mixture was concentrated in vacuo
  2. extractionThe mixture was extracted with ethyl acetate (20 ml)
  3. dry with materialdried over sodium sulphate
  4. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-892f17811ad04ed5ba0471035bfa38ca
Quelldatensatz
uspto-grants-2014_02
Patentnummer
US08658635B2

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