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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 243849Erstellt: 23. Oktober 2026

Benzoic acid, 2-bromo-5-fluoro-, methyl ester → methyl 5-fluoro-2-(1H-pyrazol-5-yl)benzoate

https://huagongshe.com/de/reaction/243849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoic acid, 2-bromo-5-fluoro-, methyl esterHCID 138875—
EduktSodium BicarbonateHCID 516892—
Edukt1H-Pyrazole-5-boronic acidHCID 11251979—
LösungsmittelWaterHCID 962—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produktmethyl 5-fluoro-2-(1H-pyrazol-5-yl)benzoateHCID 6708667844,9%

Reaktionsbedingungen

Temperatur23 °C

Reaktionsschritte

Methyl 2-bromo-5-fluorobenzoate (1.0 g, 4.2 mmol) and (1H-pyrazol-5-yl)boronic acid (485 mg, 4.6 mmol) were combined and dissolved in degassed DME (15 ml) then treated with NaHCO3 (706 mg, 8.4 mmol) in water and the reaction purged with bubbling N2 for 5 minutes. The reaction was treated with Pd(PPh3)4 (243 mg (0.2 mmol) and then purged with bubbling for 5 minutes in a sealed vessel and then heated to reflux for 2 h. The reaction mixture was cooled to 23° C., filtered, and solid rinsed with EtOAc. The organic layers were separated, dried and concentrated. Purification via FCC (ethyl acatate/hexanes, 0-30%) afforded methyl 5-fluoro-2-(1H-pyrazol-5-yl)benzoate (415 mg, 44%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653263B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-bb7166fd3d904c0d84d22df8de72cb8c
Quellennotizuspto-grants-2014_02