Synthesis of the (Z) and (E) isomers of 1,2‐diaryl‐3‐methyl‐4,5‐dioxo‐3‐pyrrolidinecarboxylic acid esters. Structural assignment by nmr and mass spectroscopy

Abstract

AbstractReaction of N‐benzylideneaniline, 1a, with 3‐methyl‐2‐oxobutanedioic acid diethyl ester, 2a, produced isomeric 3‐methyl‐4,5‐dioxo‐1,2‐diphenyl‐3‐pyrrolidinecarboxylic acid ethyl esters, 3a and 3b. The higher melting isomer, 3a, was shown to have the (Z) configuration by nmr spectroscopy. The (Z) and (E) isomers of 3‐methyl‐4,5‐dioxo‐1,2‐diphenyl‐3‐pyrrolidinecarboxylic acid methyl esters, 3c and 3d, were prepared from 1a and 3‐methyl‐2‐oxobutanedioic acid dimethyl ester, 2b. The higher melting isomer, 3c, was shown to have the (Z) configuration. Similarly, N‐benzylidene‐p‐toluidine, 1b, reacted with 2a to form (Z) and (E) isomers of 3‐methyl‐4,5‐dioxo‐1‐(4‐methylphenyl)‐2‐phenyl‐3‐pyrrolidinecarboxlic acid ethyl esters, 3e and 3f. Assignment of the 13C carbonyl carbon nmr chemical shift was made by preparing 2‐methyl‐3‐oxobutanedioic‐1‐13C acid diethyl ester, 4, and from it the corresponding (Z) and (E) isomers of 3‐methyl‐4,5‐dioxo‐1,2‐diphenyl‐3‐pyrrolidinecarboxylic 13C acid ester, 5a and 5b. The mass spectra of the (Z) isomers exhibit prominent ions corresponding to the masses of the Schiff bases used to make them, and ions corresponding to the loss of ArNCOCO from the parent ion. The (E) isomers 3b, 3d and 5b exhibit a prominent ion of mass 264; 3f gives mass 278, corresponding to the loss of the carboalkoxy group.