4-bromo-1-methyl-1H-pyrazole-5-carbaldehyde → (4-bromo-1-methyl-1H-pyrazol-5-yl)methanol

HRID 1480890

Reaktionsgleichung

Reaktionsgleichung von HRID 1480890
[Br:1][C:2]1[CH:3]=[N:4][N:5]([CH3:9])[C:6]=1[CH:7]=[O:8].[BH4-].[Na+]>CO>[Br:1][C:2]1[CH:3]=[N:4][N:5]([CH3:9])[C:6]=1[CH2:7][OH:8]

Komponenten

4

Versuchsvorschrift

To a solution of 4-bromo-1-methyl-1H-pyrazole-5-carbaldehyde (677 mg, 3.58 mmol) in MeOH (8 mL) at 0° C., NaBH4 (136 mg, 0.86 mmol) was added. The solution was stirred at room temperature for 2 hours. The reaction was concentrated in vacuo and diluted with water. The solution was extracted with EtOAc, the organic layer collected, dried over sodium sulphate and concentrated in vacuo to afford the title compound as a white solid (614 mg, 90%).

Aufarbeitung

  1. concentrationThe reaction was concentrated in vacuo
  2. additiondiluted with water
  3. extractionThe solution was extracted with EtOAc
  4. customthe organic layer collected
  5. dry with materialdried over sodium sulphate
  6. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-c8315fbc0f7541bc99a71670c81ff94d
Quelldatensatz
uspto-grants-2016_08
Patentnummer
US09409907B2

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