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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 58571Erstellt: 24. Oktober 2026

1,2-Dimethoxyethane → Ethyl 5-(2,5-difluorobenzyl)isoxazole-3-carboxylate

https://huagongshe.com/de/reaction/58571

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DimethoxyethaneHCID 8071—
EduktSodium CarbonateHCID 10340—
Edukt(2,5-Difluorophenyl)boronic acidHCID 2734335—
EduktEthyl 5-(bromomethyl)-1,2-oxazole-3-carboxylateHCID 13124955—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
ProduktEthyl 5-(2,5-difluorobenzyl)isoxazole-3-carboxylateHCID 6683191559%

Reaktionsschritte

1,2-Dimethoxyethane (8 mL) and water (2 mL) were added to the mixture of ethyl 5-(bromomethyl)isoxazole-3-carboxylate (1.00 g; 4.27 mmol), 2,5-difluorophenylboronic acid (0.773 g; 4.70 mmol), tetrakis(triphenylphosphine)palladium(0) (0.248 g; 0.640 mmol) and sodium carbonate (0.911 g; 8.55 mmol). The mixture was irradiated in a microwave oven at 130° C. for 20 minutes. After cooling, the reaction mixture was extracted with ethyl acetate and water. The organic layer was concentrated under reduced pressure and the residue was purified by flash chromatography on silica gel (eluent: 5 to 40% of ethyl acetate in heptane) to give 0.67 g (59%) of ethyl 5-(2,5-difluorobenzyl)isoxazole-3-carboxylate as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434722B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-56c06f3f570d491c85ebf3b41cfd0baa
Quellennotizuspto-grants-2016_09