Formaldehyde → 4-bromo-3-(trifluoromethyl)-1H-pyrazole-1-ylmethanol

HRID 1983017Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1983017
[Br:1][C:2]1[C:3]([C:7]([F:10])([F:9])[F:8])=[N:4][NH:5][CH:6]=1.[CH2:11]=[O:12]>CC(C)=O>[Br:1][C:2]1[C:3]([C:7]([F:10])([F:9])[F:8])=[N:4][N:5]([CH2:11][OH:12])[CH:6]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
140 °C

Versuchsvorschrift

The mixture of 3.38 g of 4-bromo-3-(trifluoromethyl)-1H-pyrazole and 0.66 g of paraformaldehyde was stirred at 140° C. for 5 hours. After the reaction mixture was cooled to room temperature, acetone was added to the reaction mixture. The mixture was filtered. Hexane was added to the residue obtained by concentration of the filtrate under reduced pressure, as a result, a crystal was formed. The crystal was collected to obtain 3.28 g of 4-bromo-3-(trifluoromethyl)-1H-pyrazole-1-ylmethanol.

Aufarbeitung

  1. temperatureAfter the reaction mixture was cooled to room temperature
  2. filtrationThe mixture was filtered
  3. additionHexane was added to the residue
  4. customobtained by concentration of the filtrate under reduced pressure, as a result
  5. customa crystal was formed
  6. customThe crystal was collected

Quellen und Nachweise

ORD-Eintrag
ord-f662bb82c3de4544a643ac2e08139b7e
Quelldatensatz
uspto-grants-2009_06
Patentnummer
US07541374B2

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