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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392864Generated: November 2, 2026

Benzoyl Peroxide → 2-tert-butyl-4-bromomethyl-5-chloro 3(2H)-pyridazinone

https://huagongshe.com/reaction/1392864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant2-tert-butyl-5-chloro-4-methylpyridazin-3-(2H)-oneHCID 13822264—
SolventCarbon TetrachlorideHCID 5943—
Product2-tert-butyl-4-bromomethyl-5-chloro 3(2H)-pyridazinoneHCID 19081406—

Reaction Steps

2-tert-butyl-4-methyl-5-chloro 3(2H)-pyridazinone (3 g, 15 mmol) is dissolved in 25 ml of carbon tetrachloride and to it is added N-bromosuccinimide (2.6 g, 15 mmol) and benzoyl peroxide (14 mg). The mixture is then refluxed for 6 hours after which it is cooled and filtered. The filtrate is washed with water and dried. After removing the organic solvent the crude residue obtained is purified by flash chromatography (silica gel; ethyl acetate/hexanes: 9:1) to obtain the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07344702B2
Source datasetuspto-grants-2008_03
ORD IDord-5eef8a562673428fa0951a9c7a109651
Source noteuspto-grants-2008_03