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HRID 629435Erstellt: 24. Oktober 2026

1,2-Dimethoxyethane → methyl 5-(4-(1H-pyrazol-1-yl)benzyl)-3-fluoro-2-hydroxy-4-methylbenzoate

https://huagongshe.com/de/reaction/629435

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DimethoxyethaneHCID 8071—
EduktSodium CarbonateHCID 10340—
Edukt1-[4-(chloromethyl)phenyl]-1H-pyrazoleHCID 7130887—
EduktMethyl 3-fluoro-2-hydroxy-4-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoateHCID 131735372—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
Produktmethyl 5-(4-(1H-pyrazol-1-yl)benzyl)-3-fluoro-2-hydroxy-4-methylbenzoateHCID 11846811014,2%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Tetrakis(triphenylphosphine)palladium(0) (0.40 g) was added to a mixture of methyl 3-fluoro-2-hydroxy-4-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (2.13 g), 1-(4-(chloromethyl)phenyl)-1H-pyrazole (1.32 g), sodium carbonate (1.46 g), DME (30.0 mL) and water (10.0 mL) under argon atmosphere, and the mixture was stirred overnight at 80° C. The reaction mixture was allowed to be cooled to room temperature, water was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (0.33 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09315458B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-e1e619c23bff4b029fcd87eabdc68dc2
Quellennotizuspto-grants-2016_04