J. Kula et al., FURTHER STUDY ON THE ONE-POT SYNTHESIS OF (E)-2-NONENAL FROM CASTOR-OIL, Journal of the American Oil Chemists' Society, 71(5), 1994, pp. 545-546
A one-step procedure is described for the synthesis of (E)-2-nonenal f
rom commercial castor oil by oxonolysis in methanol, followed by reduc
tion of the ozonide products with dimethyl sulfide and exposure of the
resulting intermediate product to dilute sulfuric acid. The developed
process allows the production of the aldehyde with a yield of 80% at
a purity of 95%. The method has advantages over all those reported ear
lier, because of inexpensive raw material and reducing agent, recyclin
g of the solvent and its unusual simplicity.