42766-36-9

Upstream product

• 104-01-8 4-Methoxyphenylacetic acid 

Downstream Products

• 132589-77-6 (4-Methoxy-phenyl)-acetic acid 1-benzoyl-propyl ester 
• 223553-31-9 2,3-dihydro-3-hydroxy-3-[(4-methoxyphenyl)methyl]-1H-isoindol-1-one 
• 3951-10-8 2-(4-methoxyphenyl)acetic anhydride 
• 55815-72-0 [¹³C₁]-4-methoxyphenyl acetic acid 
• 132590-02-4 C₃₀H₃₈N₂O₃ 
• 132590-01-3 C₂₈H₃₄N₂O₃ 
• 132590-00-2 1-{2-[4-(5-Ethyl-4-phenyl-furan-3-yl)-phenoxy]-ethyl}-pyrrolidine 
• 132589-95-8 1-{2-[4-(4-Phenyl-furan-3-yl)-phenoxy]-ethyl}-piperidine 
• 132589-94-7 1-{2-[4-(4-Phenyl-furan-3-yl)-phenoxy]-ethyl}-pyrrolidine 
• 132589-85-6 5-Ethyl-3,4-bis-(4-methoxy-phenyl)-5H-furan-2-one 
• 132589-89-0 5-Ethyl-3,4-bis-(4-hydroxy-phenyl)-5H-furan-2-one 
• 132589-83-4 5-Ethyl-3-(4-methoxy-phenyl)-4-phenyl-5H-furan-2-one 
• 132589-87-8 5-Ethyl-3-(4-hydroxy-phenyl)-4-phenyl-5H-furan-2-one 
• 132589-93-6 C₁₈H₁₆O₃ 

Relevant academic research and scientific papers

Facile and direct synthesis of symmetrical acid anhydrides using a newly prepared powerful and efficient mixed reagent

An efficient mixed reagent for direct synthesis of symmetrical carboxylic anhydrides from carboxylic acids has been prepared. Carboxylic acids are converted to anhydrides using triphenylphosphine/ trichloroisocyanuric acid under mild reaction conditions at room temperature. Short reaction time, excellent yields of products, low cost, availability of reagents, simple experimental procedure, and easy work-up of the products are the main advantages of the presented method.