TPPTS
3,3′,3′′-Phosphanetriyltris trisodium salt, is an organic compound that is also known as sodium triphenylphosphine trisulfonate. The compound has the formula P3. This white solid is an unusual example of a water-soluble phosphine. Its complexes are also water-soluble. Its complex with rhodium is used in the industrial production of butyraldehyde.
Synthesis
TPPTS is synthesized by sulfonation of triphenylphosphine. The sulfonation occurs at one meta-position of each of the three phenyl rings. The sulfonation agent is oleum, a solution of sulfur trioxide in sulfuric acid. Immediately upon dissolving in the oleum, the phosphine is protonated. It is the phosphonium salt that undergoes the sulfonation which explains its meta selectivity:As a Lewis base, tppts is stronger than triphenylphosphine.
TPPTS at the origin of two-phase homogeneous catalysis
TPPTS was first synthesized in 1975 by E.G Kuntz who was an engineer at Rhône-Poulenc with the aim of carrying out a two-phase homogeneous catalysis in which the aqueous phase catalyst could be easily separated from the reaction products and recycled. Using TPPTS, allowed him to prepare water-soluble complexes with Rh, Ni, Pd. E.G. Kuntz patented several two-phase homogeneous catalytic reactions:- hydroformylation of propylene with Rh TPPTS, later leading to the Ruhrchemie / Rhône-Poulenc process.
- hydrocyanation of olefins and dienes with Ni TPPTS.
- telomerization of butadiene to 2.7 octadiene -1-ol with Pd TPPTS.
- The Rh TPPTS catalyst was later used by D.Morel to synthesize geranylacetone from myrcene and farnesylacetone from beta-farnesene which are intermediates in the synthesis of vitamin E. This process was industrialized by Rhône-Poulenc in 1988.