Реакция #1552086

ord-f557c3b5ba314ef1b774ae19baec790e

Уравнение реакции

[Na+].[OH-]
sodium hydroxide
Cn1nc(C(F)F)c(C=O)c1Cl
5-chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carbaldehyde
Cc1ccccc1
toluene
OO
hydrogen peroxide
Cn1nc(C(F)F)c(C(=O)O)c1Cl
5-chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid
Выход 49.0%

Растворители

Условия реакции

Температура
50°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthe temperature below 37° C
  2. 2
    workup.ADDITIONAfter the end of the addition
  3. 3
    Другоеis back to room temperature
  4. 4
    Другоеthe two phases are separated
  5. 5
    Экстракцияthe organic phase is extracted with 100 ml of water
  6. 6
    ФильтрацияThe resulting white precipitate is filtered
  7. 7
    Промывкаwashed twice with 20 ml of water
  8. 8
    Другоеdried

Методика

In a 500 ml flask, 6.0 g (31 mmol) of 5-chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carbaldehyde are added to 30 ml of toluene. A solution of 2.4 g (62 mmol) of sodium hydroxide in 6 ml of water is added to the reaction mixture, followed by 103 ml of a 30% solution of hydrogen peroxide in water, whilst keeping the temperature below 37° C. After the end of the addition, the reaction mixture is stirred at 50° C. for 7 hours. Once the reaction mixture is back to room temperature, the two phases are separated and the organic phase is extracted with 100 ml of water. The combined aqueous phases are acidified to pH 2 with aqueous hydrochloric acid. The resulting white precipitate is filtered, washed twice with 20 ml of water, and dried to yield 3.2 g of 5-chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 3.78 (s, 3H); 7.12 (t, 1H, JHF=53.60 Hz) 13.19 (s, 1H); IR (KBr): 1688 cm−1 (C═O); 2200-3200 cm−1 broad (hydrogen bond).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08999956B2uspto-grants-2015_04