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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175029Generated: November 1, 2026

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

https://huagongshe.com/reaction/2175029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic acid, 2-bromo-5-fluoro-, methyl esterHCID 138875—
ReactantSodium BicarbonateHCID 516892—
Reactant1H-Pyrazole-5-boronic acidHCID 11251979—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Productmethyl 5-fluoro-2-(1H-pyrazol-5-yl)benzoateHCID 6708667844.9%

Reaction Conditions

Temperature23 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062044B2
Source datasetuspto-grants-2015_06
ORD IDord-4348045808e04cfeb7f4ea78768772da
Source noteuspto-grants-2015_06