3986-35-4

Upstream product

• 3717-22-4 (Z)-para-methoxybenzaldehyde oxime 
• 98-88-4 benzoyl chloride 
• 3717-21-3 (E)-4-methoxybenzaldoxime 
• 3717-21-3 p-methoxyl benzaldoxime 
• 94-36-0 dibenzoyl peroxide 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 874-90-8 4-methoxybenzonitrile 
• 65-85-0 benzoic acid 
• 622-73-1 4-methoxybenzaldehydephenylhydrazone 
• 3717-21-3 (E)-4-methoxybenzaldoxime 

Relevant academic research and scientific papers

Iron-catalyzed synthesis of benzoxazoles by oxidative coupling/cyclization of phenol derivatives with benzoyl aldehyde oximes

An iron-catalyzed oxidative coupling/cyclization reaction for the synthesis of benzoxazoles at room temperature is reported. This reaction was enabled by an inexpensive iron(iii) catalyst by treating readily available phenol derivatives with benzoyl aldehyde oximes. Mechanistic studies show that benzoyl aldehyde oxime is not only used as a substrate, but also serves as an ancillary ligand to support the iron salt in the promotion of the transformation.

Efficient and alternative approach for preparation of O-benzoyloximes using benzoyl peroxide

Benzoyl peroxide has been used as a mild and efficient reagent for the preparation of benzoyl ester of oxime in moderate to good yields. Copyright Taylor & Francis Group, LLC.