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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243849Generated: October 26, 2026

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

https://huagongshe.com/reaction/243849

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 numberUS08653263B2
Source datasetuspto-grants-2014_02
ORD IDord-bb7166fd3d904c0d84d22df8de72cb8c
Source noteuspto-grants-2014_02