Réaction #792151

ord-ecc3432a14c847658997e5148de2edaa

Équation de réaction

CN(C)C=O
N,N-dimethylformamide
O=C(O)c1cc(C(F)(F)F)nn1-c1ccccc1
1-phenyl-3-(trifluoromethyl)pyrazole-5-carboxylic acid
O=C(O)c1cc(C(F)(F)F)nn1-c1ccccc1
product
O=C(O)c1cc(C(F)(F)F)nn1-c1ccccc1
1-Phenyl-3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid
O=C(Cl)C(=O)Cl
oxalyl chloride
O=C(Cl)c1cc(C(F)(F)F)nn1-c1ccccc1
1-Phenyl-3-(trifluoromethyl)-1H-pyrazole-5-carbonyl chloride

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas heated
  2. 2
    Températureto reflux for a period of 35 minutes
  3. 3
    AutreVolatiles were removed
  4. 4
    Autreon a rotary evaporator at a bath temperature of 55° C

Mode opératoire

A sample of crude 1-phenyl-3-(trifluoromethyl)pyrazole-5-carboxylic acid (i.e. the product of Step B) (4.13 g, 16.1 mmol) was dissolved in methylene chloride (45 mL). The solution was treated with oxalyl chloride (1.80 mL, 20.6 mmol), followed by N,N-dimethylformamide (0.010 mL, 0.13 mmol). Off-gassing began shortly after adding the N,N-dimethylformamide catalyst. The reaction mixture was stirred for ˜20 minutes under ambient conditions, then was heated to reflux for a period of 35 minutes. Volatiles were removed by stripping the reaction mixture on a rotary evaporator at a bath temperature of 55° C. The product consisted of 4.43 g of a light-yellow oil. The only impurity observed by 1H NMR was N,N-dimethylformamide.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09173400B2uspto-grants-2015_11