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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388137Generated: November 1, 2026

Benzoyl Peroxide → 4-Bromo-7-hydroxy-2-phenyl-oxazolo[4,5-c]pyridine-6-carboxylic acid methyl ester

https://huagongshe.com/reaction/2388137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant7-Hydroxy-2-phenyl-oxazolo[4,5-c]pyridine-6-carboxylic acid methyl esterHCID 67529569—
SolventBenzeneHCID 241—
Product4-Bromo-7-hydroxy-2-phenyl-oxazolo[4,5-c]pyridine-6-carboxylic acid methyl esterHCID 8664811161%

Reaction Steps

A suspension of 7-hydroxy-2-phenyl-oxazolo[4,5-c]pyridine-6-carboxylic acid methyl ester (3.57 g, 13.2 mmol; example 1d), N-bromosuccinimide (2.47 g, 13.9 mmol), and benzoyl peroxide (320 mg, 1.32 mmol) in 43 mL of benzene was heated at reflux temperature for 5 hours. The reaction mixture was washed successively with saturated sodium bicarbonate, brine, saturated ammonium chloride solution, and brine. The organic solution was dried, filtered, and concentrated. The residue was purified by flash chromatography eluting from silica gel with a gradient of 0-25% methanol in methylene chloride to give 2.81 g of the title compound as a light yellow solid. MS: (+) m/z 348.9, 350.9 (M+1, 79Br/81Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269008B2
Source datasetuspto-grants-2012_09
ORD IDord-2861dd26dd344c899dda14ad950df6e6
Source noteuspto-grants-2012_09