Answers are grounded in this paper and cite their sources.
LiCl acts as a highly effective catalyst for cyanosilylation of various aldehydes and ketones to the corresponding silylated cyanohydrins. The reaction proceeds smoothly with a substrate/catalyst molar ratio of 100-100,000 at 20-25 degrees C under solvent-free conditions. alpha,beta-Unsaturated aldehydes are completely converted to the 1,2-adducts. The cyanation products can be isolated by direct distillation of the reaction mixture.
No takes yet. Share an insight, caveat, or question.
Kurono et al. (2005) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: