An Improved Route to Substituted Cyclopenta[c]thiophenes: Synthesis of 5-Alkyl-1,3-dimethyl-4H-cyclopenta[c]thiophenes and Sulfone Ester Precursor

Autor: Nathan C. Tice, Amber J. Bell, Joseph B. Scott, Paul J. Orosz, Chad A. Snyder, Riley G. Jones, Vineet V. Karambelkar, Jessica M. Wilson
Rok vydání: 2009
Předmět:
Zdroj: Journal of the Kentucky Academy of Science. 70:70-74
ISSN: 1098-7096
DOI: 10.3101/1098-7096-70.1.70
Popis: An improved route to substituted cyclopenta[c]thiophenes was accomplished by treating 1,3-dimethyl-5,6-dihydro-4H-cyclopenta[c]thiophene-5-one (1) with alkyl Grignard reagents to obtain the 5-alkyl-1,3-dimethyl-4H-cyclopenta[c]thiophenes, 5-methyl-1,3-dimethyl-4H-cyclopenta[c]thiophene (2) and 5-ethyl-1,3-dimethyl-4H-cyclopenta[c]thiophene (3), in good yield (60% and 65%, respectively). An important cyclopenta[c]thiophene precursor, 5-carbomethoxy-5-phenylsulfonyl–1,3-dimethyl-5,6-dihydro-4H-cyclopenta[c]thiophene (9) was synthesized, in an alternate route, by treating 3,4-bis(chloromethyl)-2,5-dimethylthiophene (7) with methyl phenyl sulfonyl acetate (8).
Databáze: OpenAIRE