106183-47-5

Upstream product

• 186581-53-3 diazomethane 
• 97677-81-1 2-(2'-chloroformylphenyl)thiophene 
• 6072-49-7 2-(2'-carboxyphenyl)thiophene 
• 615-36-1 2-bromoaniline 
• 106851-53-0 2-(2’-bromophenyl)thiophene 

Downstream Products

• 106183-49-7 5-Hydroxynaphtho<1,2-b>thiophene 
• 106851-55-2 2-thenyl(2-yl-benzoyl)azomethane 
• 106183-48-6 4,10b-dihydro-inda-<1',2'-1,2>cyclopropa<1,3-b>thiophen-6-one 
• 154191-76-1 methyl diazo<2-(3,4,5-trichloro-2-thienyl)phenyl>acetate 
• 154191-78-3 methyl <2-(3,4,5,-trichloro-2-thienyl)phenyl>acetate 
• 154191-77-2 methyl <2-(2-thienyl)phenyl>acetate 

Relevant academic research and scientific papers

Potentially Aromatic Thiophenium Ylides. V. Reactions of Ethoxycarbonyl- (and Methoxycarbonyl)-2-(2-thienyl)phenylcarbene

In an attempt to make thiophenium ylides in which the ylide bond is part of a five-membered ring annulated to the α-side of the thiophene moiety, two alkoxycarbonyl substituted 2-(2-thienyl)phenylcarbenes have been made, with and without chlorine substituents in the remaining thiophene positions.With rhodium acetate as a catalyst the carbene without chlorines cyclized to the 3-position of the thiophene to give a fluorene analogue, whereas no cyclization was detected when the 3-position was blocked.

Potentially Aromatic Thiophenium Ylides 3. Cyclization of 2-(2'-Thienyl)benzoylcarbene

Catalytic decomposition of 2(2'-diazoacetylphenyl)thiophene gives the 4,10b-dihydro-indacyclopropathiophen-6-one (5) and the naphthothiophen-5-ol (6).It is shown that 5 rearranges to 6 under acid catalysis.The mechanisms for the r