156726-87-3Relevant articles and documents
Syntheses and some chemistry of 1,2- and 1,1-bis(2-pyrrolyl)ethenes
Xie, Hong,Lee, David A.,Wallace, David M.,Senge, Mathias O.,Smith, Kevin M.
, p. 8508 - 8517 (2007/10/03)
trans-1,2-Bis(2-pyrrolyl)ethenes (e.g. 18-20) are prepared by McMurry-type reductive coupling of the corresponding 2-formylpyrroles. The isomeric 1,1-bis(2-pyrrolyl)ethenes (e.g. 24) are prepared as a minor byproduct in the reaction of 2-unsubstituted pyrroles (e.g. 22) with acetic anhydride under Friedel-Crafts conditions; the major product, as expected is the 2-acetylpyrrole 23. However, 5-(chloromethyl)dipyrromethanes (e.g. 35) can be obtained in high yield by reaction of 2-unsubstituted pyrroles 22 with chloroacetaldehyde diethyl acetal. Base-catalyzed elimination of HCl from 35 affords the 1,1-bis(2-pyrrolyl)ethene 24 along with the trans- and cis-1,2-bis(2-pyrrolyl)-ethenes 18 and 36, respectively. Conditions are optimized to afford a 66% yield of the 1,1-bis(2-pyrrolyl)ethene 24. In neutral organic solvents, 1,1-bis(2-pyrrolyl)ethenes exist in the ethene tautomeric form 2, rather than as the corresponding 5-methyldipyrromethene isomer 3; however, under acidic conditions, the 5-methyldipyrromethene salt 38 is observed, and the 5-methyl group undergoes acid-catalyzed exchange in deuterated solvents. 1,1-Bis(2-pyrrolyl)ethenes (e.g. 24) undergo standard chemistry, such as catalytic hydrogenation (Adams catalyst) of the alkene bond (to give 5-methyldipyrromethane 44), Vilsmeier formylation [to give 2-formyl-1,1-bis(2-pyrrolyl)-ethene 57], and reaction with Eschenmoser's salt (N,N-dimethyl(methylene)ammonium iodide) [to give 2-((N,N-dimethylamino)methyl)-1,1-bis(2-pyrrolyl)ethene 59]. Both the 5-methyldipyrromethane-1,9-dicarboxylic acid 45 and the 1,1-bis(5-carboxy-3,4-dimethyl-2-pyrrolyl)ethene 53 react with the 1,9-diformyldipyrromethane 46, under standard MacDonald conditions, to give 3,5,8-trimethyldeuteroporphyrin IX dimethyl ester 47.
Syntheses, Structure, Properties and Chemistry of 1,1-Di(pyrrolyl)ethenes
Xie, Hong,Lee, David A.,Senge, Mathias O.,Smith, Kevin M.
, p. 791 - 792 (2007/10/02)
Reaction of a 2-unsubstituted pyrrole with acetic anhydride and stannic chloride unexpectedly promotes self-condensation to give symmetrical di(pyrrolyl)ethene as a side-product in 6-10percent yield, but overall yields of these 1,1-di(pyrrolyl)ethenes can be improved to 66percent using a rational alternate route; structure and chemistry of 1,1-di(pyrrolyl)ethenes 2 are discussed.
