Castor, safflower, and oleic safflower oil derivatives with enhanced reactivity and hydroxyl group content were prepared by hydroformylation with a rhodium-triphenylphosphine catalyst, followed by hydrogenation. Rigid urethane foams prepared from these hydroxymethylated derivatives had excellent compressive strengths, closed cell contents, and dimensional stability. Best properties were obtained from hydroxymethylated polyol esters of castor acids.
C H 3-( CH 2)z-C H-( CH 2 )y-CH-( CH 2 )x-C OOR 176 236 303 t-© t'~ 7~ t-ro © aRef. 5. bOn methyl esters, JXR silicone column programed from 180-260 C at 2 C/rain, flame ionization detector. Hydroformylated castor esters showed several peaks which were not identified. CPrepared by hydrogenation of hydroformylated products with Raney nickel at 100 C/1000 psig H 2. dOn acetate esters, eCalculated values for methyl hydroxymethylstearate = 170.5; methyl dihydroxymethylstearate = 312.5; methyl hydroxymethylhydroxystearate = 325. fEquivalent wt = 56,100/(hydroxyl value + acid value). < © r~