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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861879Generated: November 2, 2026

Benzoyl Peroxide → 4-(Bromomethyl)-2,6-di-tert-butylpyridine

https://huagongshe.com/reaction/1861879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant2,6-Di-tert-butyl-4-methylpyridineHCID 98898—
Reactant2,6-Di-tert-butylisonicotinic acidHCID 4736941—
Product4-(Bromomethyl)-2,6-di-tert-butylpyridineHCID 12930888—

Reaction Steps

Reaction Scheme 13 provides an example for the preparation of 2,6-di-tert-butylisonicotinic acid (Compound C3) which is a reagent in accordance with Formula 8 for the preparation of several preferred compounds of the present invention. Thus, 2,6-di-tert-butyl-4-methylpyridine (available commercially from Aldrich Chemical Co.) is reacted with N-bromosuccinimide and benzoyl peroxide to provide 4-bromomethyl-2,6-di-tert-butylpyridine (Compound A3). Compound A3 is reacted with base (sodium hydroxyde) to yield the coresponding hydroxymethyl compound (Compound B3), which is thereafter oxidized in a Jones oxidation reaction to give 2,6-di-tert-butylisonicotinic acid (Compound C3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06534544B1
Source datasetuspto-grants-2003_03
ORD IDord-795cccd28ba9473784cfd96f09f26e30
Source noteuspto-grants-2003_03