230285-32-2

Upstream product

• 89358-46-3 4-hydroxy-3-methylbutan-2-one ethylene acetal 
• 27773-09-7 carbethoxy-1 ethylene dioxy-2 methyl-1 propane 
• 609-14-3 2-acetylpropanoic acid ethyl ester 

Downstream Products

• 230285-47-9 4-methyl-1-phenyl-1-(2-tetrahydropyranyloxy)-5-pentanol 
• 230285-48-0 4-methyl-1-phenyl-5-(N-phthalimidoxy)-1-(2-tetrahydropyranyloxy)pentane 
• 230285-46-8 5-(tert-butyldiphenylsiloxy)-4-methyl-1-phenyl-1-(2-tetrahydropyranyloxy)pentane 
• 230285-36-6 5-(tert-butyldiphenylsiloxy)-4-methyl-1-phenyl-1-(2-tetrahydropyranyloxy)-3-pentanone 
• 230285-44-6 5-(tert-butyldiphenylsiloxy)-4-methyl-1-phenyl-1-(2-tetrahydropyranyloxy)-3-pentanol 
• 230285-45-7 O-[5-(tert-butyldiphenylsiloxy)-4-methyl-1-phenyl-1-(2-tetrahydropyranyloxy)-3-pentyl]-S-methyl dithiocarbonate 
• 230285-49-1 4-methyl-1-phenyl-5-(N-phthalimidoxy)-1-pentanol 
• 230285-50-4 4-methyl-1-phenyl-1-(diphenylphosphatoxy)-5-(N-phthalimidoxy)pentane 

Relevant academic research and scientific papers

Synthesis of tetrahydrofurans by a tandem hydrogen atom abstraction/ radical nucleophilic displacement sequence

(equation presented) The reaction of a series of 5-(N-phthalimidoxy)-1-phenyl-1-(diphenylphosphatoxy)pentanes with triphenyltin hydride and AIBN provides alkoxy radicals which undergo 1,5-hydrogen atom abstraction to give β-(phosphatoxy)alkyl radicals. These radicals then take part in a radical nucleophilic displacement leading, after chain transfer, to tetrahydrofurans.