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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238360Erstellt: 25. Oktober 2026

Dimethylformamide → 1-Methyl-5-{[4-(trifluoromethyl)phenyl]ethynyl}-1H-pyrazole

https://huagongshe.com/reaction/238360

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
Edukt1-Ethynyl-4-(trifluoromethyl)benzeneHCID 4348295—
Edukt5-Iodo-1-methyl-1H-pyrazoleHCID 13334065—
KatalysatorTriphenylphosphineHCID 11776—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelWaterHCID 962—
Produkt1-Methyl-5-{[4-(trifluoromethyl)phenyl]ethynyl}-1H-pyrazoleHCID 8668486380,5%

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

A mixture of 5-iodo-1-methyl-1H-pyrazole (8.00 g), 1-ethynyl-4-(trifluoromethyl)benzene (6.54 g), copper(I) iodide (110 mg), bis(triphenylphosphine)palladium(II) dichloride (1.35 g), triphenylphosphine (504 mg), triethylamine (8.00 mL) and dimethylformamide (70 mL) was stirred at 75° C. for 2 hours. Thereafter, the reaction solution was added to water, and the obtained mixture was then extracted with ethyl acetate. The organic layer was successively washed with water and a saturated saline, and was then dried over anhydrous magnesium sulfate, followed by vacuum concentration. The residue was purified by column chromatography (silica gel cartridge, hexane:ethyl acetate=85:15 to 75:25), so as to obtain the title compound (7.74 g) in the form of a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642626B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-2746452428f0474e8b37d0e24d47a569
Quellennotizuspto-grants-2014_02