Reaction of 1,3-dimethyl pyrimidine-(1H,3H,5H)-2,4,6-trione (1,3-dimethyl barbituric acid) with cyanogen bromide and aromatic dialdehydes in the presence of N-methyl Morpholine leads to the selective and efficient formation of a novel class of bifunctionalized linkaged heterocyclic stable bis-spiro [furo[2,3-d] pyrimidine-6,5'-pyrimidine] 2,2',4,4',6'(3H,3'H,5H)-pentaones which are dimeric forms of barbiturate (uracil and thiouracil derivatives) at the range of 0oC to ambient temperature. Structure elucidation was carried out by 1H NMR, 13C NMR and FT-IR spectroscopy. A proposed mechanism was discussed for the formation of products.