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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 406597Erstellt: 23. Oktober 2026

Methylhydrazine → ethyl 5-(2,6-difluorophenyl)-1-methyl-1H-pyrazole-3-carboxylate

https://huagongshe.com/de/reaction/406597

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethylhydrazineHCID 6061—
EduktDiethyl OxalateHCID 7268—
Edukt1-(2,6-Difluorophenyl)ethan-1-oneHCID 83643—
EduktSodium t-butoxideHCID 23676156—
LösungsmittelEthanolHCID 702—
Produktethyl 5-(2,6-difluorophenyl)-1-methyl-1H-pyrazole-3-carboxylateHCID 6661394012,5%

Reaktionsschritte

To a mixture of 2,6-difluoroacetophenone (4.7 g, 0.03 mol) and 1,2-diethyl ethanedioate (4.8 g, 0.033 mol) in ethanol (33 mL) was added sodium tert-butoxide (3.17 g, 0.033 mol). After 1 h, more ethanol (30 mL) was added to the reaction mixture and stirring was continued for 1 h. The reaction mixture was partitioned between hydrochloric acid (1 N) and diethyl ether. The organic phase was separated, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to half its original volume. To the resulting mixture was added methylhydrazine (1.52 g, 0.033 mol) and stirring was continued overnight. The reaction mixture was concentrated under reduced pressure and the resulting material was purified by silica gel chromatography (5 to 20% gradient of ethyl acetate in methylene chloride as eluant) to provide the title compound as a solid (1.0 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754115B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-346fa9d45dff41edac41bda2c0541f34
Quellennotizuspto-grants-2014_06