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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661971Generated: October 29, 2026

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

https://huagongshe.com/reaction/1661971

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 numberUS08030302B2
Source datasetuspto-grants-2011_10
ORD IDord-2834e9e657a443aabaa3f6184b648543
Source noteuspto-grants-2011_10