79328-68-0

Upstream product

• 79313-57-8 methyl 4-(ethylthio)-2,2-diphenylbutyrate 
• 956-89-8 3,3-Diphenyl-dihydro-furan-2-one 
• 71057-16-4 4-(ethylthio)-2,2-diphenylbutyric acid 
• 74-96-4 ethyl bromide 

Downstream Products

• 857198-56-2 2,2-diphenyl-butyryl chloride 
• 110050-22-1 2,2-diphenyl-butyric acid-(3-dimethylamino-propyl ester) 
• 113181-88-7 2,2-diphenyl-butyric acid-(3-dimethylamino-1-methyl-propyl ester) 
• 4226-57-7 2,2-diphenylbutanoic acid 

Relevant academic research and scientific papers

Hard Acid and Soft Nucleophile Systems. 5. Ring-Opening Reaction of Lactones to ω-Alkylthio or ω-Arylthio Carboxylic Acids with Aluminum Halide and Thiol

Lactones were converted into ω-alkylthio carboxylic acids in high yields through ω-carbon-oxygen bond cleavage when they were treated with aluminun halide and alkanethiol.The aluminum halide and arenethiol system has also been found to be useful for the preparation of the synthetically valuable ω-arylthio carboxylic acids from lactones.