Formation of phosphonates and pyrophosphates in the reactions of chlorophosphate esters with strong organic bases

Abstract

The compounds S(6-t-Bu-4-Me-C6H2O)2P(O)Cl (1), CH2(6-t-Bu-4-Me-C6H2O)2P(O)Cl (2) and (2,2′-C20H12O2)P(O)Cl (3) react with diazabicycloundecene (DBU) to give rise to, predominantly, the phosphonate compounds [S(6-t-Bu-4-Me-C6H2O)2P(O)(DBU)] +[Cl]- (4), [CH2(6-t-Bu-4-Me-C 6H2O)2P(O) (DBU)]+[Cl]- (5) and [(2,2′-C20H12O2)P(O)(DBU)] +[Cl]- (6). The first two compounds could be isolated in the pure state. In analogous reactions of 1 and 2 with diazabicyclononene (DBN) or N-methyl imidazole, only the pyrophosphates [S(6-t-Bu-4-Me-C 6H2O)2P(O)]2O (7) and [CH 26-t-Bu-4-Me-C6H2O)2P(O)] 2O (8) could be isolated, although the reaction mixture showed several other compounds in the phosphorus NMR. A possible pathway for the formation of phosphonate salts is proposed. The X-ray crystal structures of 4, 7 and 8 are also discussed.