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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1822644Erstellt: 25. Oktober 2026

Tetrahydrofuran → Allyl 2-{3-(2,6-difluorophenyl)pyrazol-1-yl}-3-(5-chloro-1-methyl-3-trifluoromethylpyrazol-4-yl)-3-hydroxyacrylate

https://huagongshe.com/reaction/1822644

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
Edukt5-Chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbonyl chlorideHCID 2794585—
EduktAllyl 2-(3-(2,6-difluorophenyl)pyrazol-1-yl)acetateHCID 22169508—
EduktPotassium butoxideHCID 23699084—
LösungsmittelWaterHCID 962—
ProduktAllyl 2-{3-(2,6-difluorophenyl)pyrazol-1-yl}-3-(5-chloro-1-methyl-3-trifluoromethylpyrazol-4-yl)-3-hydroxyacrylateHCID 86590230—

Reaktionsschritte

Potassium butoxide (0.5 g) was added to a THF (10 mL) solution of allyl 2-{3-(2,6-difluorophenyl)pyrazol-1-yl}acetate (0.5 g) and 5-chloro-1-methyl-3-trifluoromethylpyrazole-4-carbonyl chloride (0.44 g) at 0° C., and stirred for 5 minutes. Water (5 ml) was added thereto, and then extracted with diluted hydrochloric acid and ethyl acetate. After the organic layer was dried over anhydrous magnesium sulfate, and then concentrated, and the resulting concentrate was purified through silica gel column chromatography (chloroform) to obtain the intended product, Compound No. I-133 (0.89 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07037880B2
Quelldatensatzuspto-grants-2006_05
ORD IDord-1b13ba0bcd2e41769c1748fcfab9e61a
Quellennotizuspto-grants-2006_05