102285-67-6

Upstream product

• 10169-55-8 1-[4-(phenylthio)phenyl]ethan-1-one 
• 102285-64-3 α-methyl-α-furfuryl alcohol 

Downstream Products

• 102285-72-3 cis-6-methoxy-2--2-methyl-2H-pyran-3(6H)-one 
• 145371-64-8 1-ethyl-5-methyl-5--6-hydroxyperhydropyrano<3,2-d>oxazole-2-one 
• 133150-06-8 1,5-dimethyl-5<4-(phenylthio)phenyl>perhydropyrano<3,2-d>oxazole-2,6-dione-6-oxime 
• 133150-03-5 1,5-dimethyl-5-<4-(phenylthio)phenyl>-dihydro<1H,7H>-5H-pyrano<3,2-d>oxazole-2,6-dione 
• 133150-05-7 1,5-dimethyl-5-<4-(phenylthio)phenyl>-6-hydroxyperhydropyrano<3,2-d>oxazole-2-one 
• 102285-71-2 trans-6-methoxy-2--2-methyl-2H-pyran-3(6H)-one 
• 145371-48-8 2--2-methyl-6-<<(ethylamino)carbonyl>oxy>-3-oxo-3,6-dihydro-2H-pyran 
• 145371-52-4 5--1-ethyl-5-methyldihydro-<1H,7H>-5H-pyrano<3,2-d>oxazole-2,6-dione 
• 133150-04-6 2--2-methyl-6-<<(methylamino)carbonyl>oxy>-3-oxo-3,6-dihydro-2H-pyran 

Relevant academic research and scientific papers

Products from Furans. 4. Selective Oxidation of 2-Furfuryl Alcohol Derivatives, in the Presence of Aryl Thioethers, with N-Bromosuccinimide (NBS). A New Procedure for the Preparation of 2H-Pyran-3(6H)-ones

A new general fast method (as fast as a titration) for converting 2H-furfuryl alcohols of 2H-pyran-3(6H)-ones by the use of NBS as an oxidant is presented.NBS oxidizes selectively the furfuryl alcohols without affecting thioether substituents.