5554-27-8

Upstream product

• 526-75-0 2,3-Dimethylphenol 
• 98-88-4 benzoyl chloride 
• 95-47-6 o-xylene 
• 94-36-0 dibenzoyl peroxide 

Downstream Products

• 368863-12-1 3-benzoyloxy-5-tert-butyl-o-xylene 
• 65-85-0 benzoic acid 
• 116544-62-8 [2,3-Dimethyl-6-(4-methyl-benzoyl)-phenoxy]-phenyl-acetic acid ethyl ester 
• 116544-72-0 [2,3-Dimethyl-6-(4-methyl-benzoyl)-phenoxy]-phenyl-acetic acid 
• 16762-05-3 3,4,4'-Trimethyl-2-hydroxy-benzophenon 
• 16762-18-8 6,7-dimethyl-2-phenyl-3-p-tolyl-benzofuran 
• 173098-44-7 5-(benzoyloxy)-2,3-dicyanonaphthalene 

Relevant academic research and scientific papers

Solid-Phase Benzoylation of Phenols and Alcohols in Microwave Reactor: An Ecofriendly Protocol

An efficient solid-phase benzoylation of phenols and alcohols was developed under microwave irradiation. A stoichiometric amount of benzoyl chloride was sufficient to carry out the reaction. This benzoylation features short reaction time, good yields, and easy workup procedures. Furthermore, the scope of the reaction was extended to prepare 3,5-dinitrobenzoyl derivatives of alcohols.

Visible-light-triggered direct benzoyloxylation of electron-rich arenes at room temperature without chelation assistance

A RuII photocatalytic method was developed for the direct mono-benzoyloxylation of electron-rich aromatic and heteroaromatic systems even with an excess amount of benzoyl peroxide. The reaction was conducted at room temperature under visible light. The direct ArC-H benzoyloxylations occur without the assistance of any directing groups and can also tolerate various functional groups that have already shown diverse reactivities in transition-metal catalysis.