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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 990743Erstellt: 26. 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/990743

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
PatentnummerUS06462049B1
Quelldatensatzuspto-grants-2002_10
ORD IDord-af3d016ba4b84913ad02bef40af1494c
Quellennotizuspto-grants-2002_10