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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195487Generated: October 30, 2026

1,2-Difluoro-4-nitrobenzene → 6-bromo-5-(2-fluoro-4-nitrophenoxy)-1H-indazole

https://huagongshe.com/reaction/2195487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Difluoro-4-nitrobenzeneHCID 123053—
ReactantLithium ChlorideHCID 433294—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Bromo-1H-indazol-5-olHCID 59159946—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product6-bromo-5-(2-fluoro-4-nitrophenoxy)-1H-indazoleHCID 6676715350.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 6-bromo-5-hydroxy-1H-indazole (7.0 g, 33.0 mmol), 3,4-difluoronitrobenzene (4.98 mg, 31.0 mmol), NaHCO3 (2.5 g, 31.0 mmol) in DMF (100 mL) is stirred at 80° C. for 4 hours. Then LiCl (10% aqueous solution) is added and the solution is extracted with EtOAc. The organic phase is dried over anhydrous MgSO4, filtered and concentrated. The residue is purified by silica gel column chromatography eluting with PE:DCM (1:1) to give the desired product (5.5 g, 46.6% yield). MS (m/z): 354.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE043878E1
Source datasetuspto-grants-2012_12
ORD IDord-a8610b737ad041e69731241ff6d2b91e
Source noteuspto-grants-2012_12