34239-40-2

Upstream product

• 2052-01-9 2-bromo-2-methylpropionic acid 
• 98-86-2 acetophenone 
• 79-31-2 isobutyric Acid 

Downstream Products

• 35947-67-2 3,3,4-trimethyl-4-phenyl-oxetan-2-one 
• 769-57-3 α,β,β-trimethylstyrene 
• 108773-65-5 3,4-Dibromo-2-methyl-3-phenyl-but-2-yl-hydroperoxide 
• 108773-82-6 3-Bromomethyl-4,4-dimethyl-3-phenyl-[1,2]dioxetane 
• 108773-66-6 3-Bromo-3-methyl-2-phenyl-but-2-yl-hydroperoxide 
• 108773-58-6 2-methyl-3-phenylbut-1-ene-3-yl hydroperoxide 
• 108773-57-5 2-methyl-3-phenylbut-3-ene-2-yl hydroperoxide 
• 108773-71-3 3,3,4-Trimethyl-4-phenyl-[1,2]dioxetane 

Relevant academic research and scientific papers

Reaction de Reformatsky a froid avec des α-bromoesters-acetals. I. Une methode generale pour la synthese des β-hydroxyacides a partir des α-bromoesters de tetrahydropyrannyle (Note de laboratoire)

The readily accessible tetrahydropyranyl esters of α-bromoacids can be used in the Reformatsky reaction for the preparation of β-hydroxyacids.The reaction is generally carried out in cold tetrahydrofuran.The β-hydroxyacids can be easily obtained by stirring the cold solution of their tetrahydropyranyl esters with dilute hydrochloric acid.