Réaction #1552089

ord-b1253579add1474993072992075c764f

Équation de réaction

Cn1nc(C(F)F)c(C(=O)O)c1F
3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid
O=S(Cl)Cl
thionyl chloride
Cn1nc(C(F)F)c(C(=O)Cl)c1F
3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carbonyl chloride

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureAfter cooling down
  2. 2
    Autrethe reaction mixture is evaporated under vacuum

Mode opératoire

9.1 g of 3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid and 75.5 ml of thionyl chloride are refluxed for 1.5 hours. After cooling down, the reaction mixture is evaporated under vacuum to yield 10 g of 3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carbonyl chloride as a yellow oil. GC-MS; observed M/z: Molecular ion: (M+)=212; fragments: (M+-Cl)=177 and (M+-F)=193.

Source

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