4,4,4-Trifluoro-1-(2-furanyl)-1,3-butanedione → 1-(2-Chlorophenyl)-5-(furan-2-yl)-3-(trifluoromethyl)-1H-pyrazole

Temperatur

60 °C

To a mixture of 12.96 g of 4,4,4-trifluoro-1-(2-furyl)-1,3-butanedione, 8.56 g of sodium acetate and 40 ml of acetic acid was added 11.26 g of 2-chlorophenylhydrazine hydrochloride at room temperature. The mixture was stirred at 60° C. for 1 hour, and concentrated under reduced pressure. After the reaction mixture was concentrated under reduced pressure and water was poured into the residue, the mixture was extracted with chloroform three times. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried over magnesium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to obtain 18.43 g of 1-(2-chlorophenyl)-5-(2-furyl)-3-trifluoromethyl-1H-pyrazole of the formula:

1. concentrationconcentrated under reduced pressure
2. concentrationAfter the reaction mixture was concentrated under reduced pressure and water
3. additionwas poured into the residue
4. extractionthe mixture was extracted with chloroform three times
5. washwashed with an aqueous saturated sodium chloride solution
6. dry with materialdried over magnesium sulfate
7. concentrationconcentrated under reduced pressure

ORD-Eintrag

ord-f9b7dcad17d94a3ab65ed3021aada78c

Quelldatensatz

uspto-grants-2011_01

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07867949B2