Réaction #1552088

ord-bd2d37d2318b44cdb0c594b036721d57

Équation de réaction

Cl
hydrochloric acid
[Na]
sodium
Cn1nc(C(F)F)c(C(=O)F)c1F
3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carbonyl fluoride
O=S1(=O)CCCC1
tetra-hydrothiophene-1,1-dioxide
Cn1nc(C(F)F)c(C(=O)O)c1F
3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONThe temperature is kept below 20° C. during the addition
  2. 2
    FiltrationThe resulting white precipitate is filtered
  3. 3
    Lavagewashed with water
  4. 4
    Autredried

Mode opératoire

To 400 ml of a 1N sodium hydroxyde aqueous solution, is added dropwise 67.5 g of a solution (10% molar) of 3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carbonyl fluoride in tetra-hydrothiophene-1,1-dioxide. The temperature is kept below 20° C. during the addition. After 2 hours of stirring at room temperature, the reaction mixture is carefully acidified to pH 2 with concentrated aqueous hydrochloric acid. The resulting white precipitate is filtered, washed with water, and dried to yield 6 g of 3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 3.90 (s, 3H); 7.22 (t, 1H, JHF=53.55 Hz); 13.33 (s, 1H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08999956B2uspto-grants-2015_04