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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377511Generated: November 1, 2026

Benzoyl Peroxide → 1-Acetyl-3-bromomethyl-6-fluoro-1H-indazole

https://huagongshe.com/reaction/1377511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant1-(6-Fluoro-3-methyl-1H-indazol-1-yl)ethanoneHCID 22876665—
SolventCarbon TetrachlorideHCID 5943—
Product1-Acetyl-3-bromomethyl-6-fluoro-1H-indazoleHCID 2287666165%

Reaction Conditions

Temperature70 °C

Reaction Steps

1-Acetyl-6-fluoro-3-methyl-1H-indazole (5.77 g, 33.1 mmol) in CCl4 (100 mL) was treated with NBS (3.64 g, 20 mmol) and benzoyl peroxide (0.388 g, 1.6 mmol) and the mixture was heated at 70° C. for 6 h. The mixture was concentrated and the residue quickly filtered through a plug of flash silica eluting with 2%→7% EtOAc in hexane to give the crude title compound (2.97 g, 65%) contaminated with traces of dibromide and starting material. This was conveniently used directly in subsequent reactions without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665732
Source datasetuspto-grants-1997_09
ORD IDord-48669fab0a64479fa019f8dd00636f47
Source noteuspto-grants-1997_09