CYANOSILYLATION OF CARBONYL COMPOUNDS IS AN EFFICIENT PROCEDURE FOR THE SYNTHESIS OF SILYLATED CYANOHYDRINS, WHICH ARE READILY CONVERTED TO SEVERAL SIGNIFICANT BUILDING BLOCKS SUCH AS A-HYDROXY ACIDS, A-HYDROXY ALDEHYDES, 1, 2 DIOLS, A-AMINO ALCOHOLS ETC. SEVERAL REAGENTS INCLUDING LEWIS ACIDS, LEWIS BASES, METAL ALKOXIDES, BIFUNCTIONAL CATALYSTS, IODINE AND INORGANIC SALTS HAVE BEEN FOUND TO EFFECTIVELY TRANSFER THE CYANO GROUP FROM TMSCN TO CARBONYL COMPOUNDS [1, 2]. METAL-ORGANIC FRAMEWORKS (MOFS) ARE BEING RECOGNIZED AS VERY PROMISING MULTIFUNCTIONAL MATERIALS WITH THEIR HIGHLY POROUS STRUCTURES AND UNIQUE PROPERTIES. THERE IS ESPECIALLY A GROWING INTEREST IN THE USE OF MOFS AS CATALYSTS [3, 4]. RECENTLY MORE ATTENTION HAS BEEN DEDICATED OVER MAGNETIC PROPERTIES THAT HELP RAPID AND EASY SEPARATION OF THE CATALYST USING AN EXTERNAL MAGNETIC FIELD [5]. HERE WE REPORT INVESTIGATION OF MAGNETIC METAL ORGANIC FRAMEWORK CATALYTIC ACTIVITY IN THE CYANOSILYLATION OF ALDEHYDES.