| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 40174 | Applied Catalysis A: General | 2014 | 9 Pages |
•Heck arylation of acrolein diethylacetal to aldehydes or acids in water media.•Selectivity is controlled through the nature of the base.•Cinnamaldehydes are obtained in the presence of sodium acetate.•3-Arylpropionic acids are obtained in the presence of diisopropylamine.•The use of RAME-β-CD as mass transfer additive allowed increasing the reaction rate.
The selective Heck arylation of acrolein diethyl acetal catalysed by [Pd(NH3)4]Cl2 in the presence of RAME-β-CD in water as solvent is described. Depending on the base (i.e. NaOAc or HN(i-Pr)2) good to high selectivity's towards, respectively, the cinnamaldehydes 2 or the 3-arylpropionic esters 1 were achieved. The results support that depending on the base different palladium intermediate complexes are formed. Using NaOAc, {[ArPdX(H2O)2]} complex is preferentially generated giving the cinnamaldehyde 2. On the other hand, in the presence of HN(i-Pr)2, a L-type ligand, [ArPdX(HN(i-Pr)2(H2O)] or [ArPdX(HN(i-Pr)2(HN(i-Pr)2)] will be generated leading to the formation of the 3-arylpropionic ester 1. For the last, coordinated amine participates very probably to the formation of the esters through intramolecular syn β-H elimination.
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