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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230148Generated: October 30, 2026

2,4-Difluorophenol → HCID 178505881, compound

https://huagongshe.com/reaction/230148

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DifluorophenolHCID 123051—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178477865HCID 178477865—
ProductHCID 178505881HCID 17850588116.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

2,4-Difluorophenol (517 mg, 4 mmol) was placed in a 10 mL microwave reactor tube under nitrogen and cooled in an ice bath. Potassium t-butoxide (4 mL of 1.0 M solution in THF) was added dropwise, and the solution was stirred for five minutes at 0° C. The reaction mixture was warmed to room temperature, and 6-chloro-3-(2-chloro-phenyl)-1H-pyrazolo[3,4-b]pyridine (350 mg, 1.33 mmol) was added in one portion. The reaction was then heated to 160° C. via microwave for nine hours. The reaction mixture was cooled and partitioned between water and ethyl acetate. The organic phase was washed with brine, followed by water, and then dried over MgSO4. The solvent was removed under reduced pressure, and the residue was eluted through a FLASH column using 0.5% MeOH in methylene chloride. Solvent was removed, and the residue was recrystallized from methylene chloride/hexanes to afford 78 mg of 3-(2-Chloro-phenyl)-6-(2,4-difluoro-phenoxy)-1H-pyrazolo[3,4-b]pyridine as a white solid. Mass Spec. M+H=358.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566708B2
Source datasetuspto-grants-2009_07
ORD IDord-09ac2cd859ed403d88adb4704d7e04da
Source noteuspto-grants-2009_07