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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 573112Erstellt: 26. Oktober 2026

Dimethylformamide → Methyl 2-(6-chloro-5-fluoropyridin-3-yloxy)-4-fluorobenzoate

https://huagongshe.com/reaction/573112

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktMethyl 2,4-DifluorobenzoateHCID 2782897—
EduktPotassium tert-butoxideHCID 23665647—
Edukt2-Chloro-3-fluoro-5-hydroxypyridineHCID 40424737—
Lösungsmittel2-MethyltetrahydrofuranHCID 7301—
LösungsmittelEthyl AcetateHCID 8857—
ProduktMethyl 2-(6-chloro-5-fluoropyridin-3-yloxy)-4-fluorobenzoateHCID 86642876—

Reaktionsschritte

To a solution of 6-chloro-5-fluoropyridin-3-ol (0.977 g) in 2-methyltetrahydrofuran (12 mL) was added potassium 2-methylpropan-2-olate (1.0M in tetrahydrofuran, 7.28 mL). After stirring for 15 minutes at room temperature, methyl 2,4-difluorobenzoate (1.710 g) was added as a solution in 2-methyltetrahydrofuran (2 mL) followed by N,N-dimethylformamide (2 mL) then the reaction was heated to 75° C. under a nitrogen atmosphere. After stirring overnight the reaction was cooled, diluted with ethyl acetate (100 mL) and washed with water (50 mL) and brine (50 mL), dried over magnesium sulfate, filtered, and concentrated. Silica gel chromatography (GraceResolv 40 g) eluting with a gradient of 2% to 15% ethyl acetate/hexanes gave the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09029404B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-83abc5fa911a4bf9b6f6b3b079582642
Quellennotizuspto-grants-2015_05