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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956371Generated: November 2, 2026

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

https://huagongshe.com/reaction/1956371

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 numberUS05780475
Source datasetuspto-grants-1998_07
ORD IDord-33b9c4ef7e20440181ed8ebe81a64e00
Source noteuspto-grants-1998_07