69520-31-6

Basic information

• Product Name: 1-phenacyl-2,5-dihydrothiophenium bromide
• Synonyms: 1-phenacyl-2,5-dihydrothiophenium bromide
• CAS NO: 69520-31-6
• Molecular Weight: 285.205
• Mol File: 69520-31-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-phenacyl-2,5-dihydrothiophenium bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenacyl-2,5-dihydrothiophenium bromide(69520-31-6)
• EPA Substance Registry System: 1-phenacyl-2,5-dihydrothiophenium bromide(69520-31-6)

Safety Data

• Hazardous Substances Data: 69520-31-6(Hazardous Substances Data)

Upstream product

• 1708-32-3 2,5-dihydro-thiophene 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 50742-77-3 2-benzoyl-5-phenyl-2H-1,3-oxathiole 
• 2516-22-5 1-(2-(1-phenylethoxy)ethyl)benzene 
• 98-85-1 1-Phenylethanol 
• 50742-76-2 benzoyl-(2,5-dihydrothiophenio)methanide 

Relevant articles and documents

Base Catalysed Rearrangements Involving Ylide Intermediates. Part 9. The Rearrangement Reactions of Cyclic Allylic Ammonium and Sulphonium Ylides

The allylic ammonium ylides (22) and (47) and sulphonium ylide (53) are isolable, usually as crystalline solids, because their sigmatropic rearrangements are inhibited by the strain associated with the bicyclic transition state of a concerted reaction mechanism.The tetrahydropyridinium (22) and dihydrothiopyranium (29) ylides undergo a thermal rearrangement, but the pyrrolinium ylide (47) rearranges by a , rather than a , sigmatropic pathway.The dihydrothiophenium ylide (53) does not undergo either a or sigmatropic rearrangement but instead reacts in a bimolecular fashion to give eventually buta-1,3-diene, 2,5-dihydrothiophen, and the heterocycle (55).The rearrangements of the ylides (22) and (29) follow predominantly an endo-pathway leading to a single diastereomer of the products (23) and (31); this strong endo preference is not shown by analogous acyclic ammonium ylides.