Synlett 2007(2): 0330-0332  
DOI: 10.1055/s-2007-968005
LETTER
© Georg Thieme Verlag Stuttgart · New York

Pd/P(t-Bu)3: A Mild Catalyst for Selective Reduction of Alkenes under ­Transfer-Hydrogenation Conditions

Jean Michel Brunel*
Laboratoire Synthèse et Etude de Substances Naturelles à Activités Biologiques (SESNAB), Faculté des Sciences et Techniques de St Jérôme, Case 342, Université Paul Cézanne, Aix-Marseille III, Avenue Escadrille Normandie Niémen, 13397 Marseille cedex 20, France
e-Mail: bruneljm@yahoo.fr;
Further Information

Publication History

Received 15 September 2006
Publication Date:
24 January 2007 (online)

Abstract

A new and efficient mild Pd/P(t-Bu)3 catalyst for selective reduction of various alkenes under transfer-hydrogenation conditions has been developed leading to the corresponding saturated derivatives in chemical yields varying from 65% to 98%.

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Selective Reduction of 4-Allylanisole(1) under Transfer Hydrogen Conditions; General Procedure (Table 1, Entry 4): CAUTION: All reagents (solvent, phosphine ligand, formic acid) must be purified before use in order to obtain good conversions and reproducible results. In a two-necked round-bottomed flask placed under argon was added Pd(OAc)2 (5.4 mg, 2.4 × 10-5 mol) at 20 °C in freshly distilled anhyd THF (5 mL). To this solution, P(t-Bu)3 (20 mg, 10-4 mol; purchased from Acros) was successively added and the solution was heated to reflux for 10 min. To this mixture 4-allylanisole (1; 148 mg, 10-3 mol) and formic acid (230 mg, 5 × 10-3 mol) were added. The resulting solution was stirred for 15 min to reflux and then cooled to 20 °C for 12 h. After filtration over Celite and evaporation of the solvents, the crude residue was purified by chromatog-raphy on a silica gel column using PE-EtOAc (100:0 → 50:50) as eluent affording the expected product 2 in 95% yield.

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Kinetic experiments performed on the selective reduction of 4-allylanisole (1) under transfer-hydrogenation conditions indicate that such a reaction takes place in less than 4 h. Nevertheless, this reaction time seems to be highly substrate-dependent and we have chosen to perform all experiments for 12 h.