Next Article in Journal
Citotoxic Activity of Extracts and Sesquiterpene Lactones from Stachycephalum argentinum
Previous Article in Journal
Synthesis and In Vitro Antigungal Properties of 4-Aryl-4-Narylamine-1-butenes and Related Compounds
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Abstract

SRN1 and Stille Reactions: A New Synthetic Strategy

INFIQC. Depto. de Química Orgánica. Facultad de Ciencias Químicas. UNC. 5000 – Córdoba, Argentina
*
Author to whom correspondence should be addressed.
Molecules 2000, 5(3), 431-432; https://doi.org/10.3390/50300431
Published: 22 March 2000

Abstract

:
The photostimulated reaction of Me3Sn- ion with mono, di and trichloro arenes in liquid ammonia gave very good yields of stannanes by the SRN1 mechanism. These products reacted by a palladium-catalized cross coupling reaction with halobenzenes to give phen-ylated products also in very goods yields. Similar yields can be obtained in one-pot reac-tions.

Introduction

The radical nucleophilic substitution, or SRN1 reaction, is a process through which a nucleophilic substitution is obtained [1]. The scope of the process has considerably increased and nowadays it is an important synthetic possibility to achieve substitution of different substrates. Several nucleophiles can be used, such as carbanions and anions from compounds bearing heteroatoms, which react to form new C-C or C-heteroatom bonds in good yields. We thought that the photostimulated reaction of mono-, di-and trichloro- arenes with Me3Sn- ions in liquid ammonia to synthesize the trimethylarylstannanes followed by the Pd(0) cross coupling reaction with haloarenes (Stille Reaction) [2,3] would be an im-portant approach for the synthesis of arylated or polyarylated compounds [4]. Thus, we undertook the study of the palladium catalyzed reaction of trimethylarylstannanes, synthesized by the SRN1 mecha-nism, with mono-, di- and trichloro- arenes as a model reaction for this methodology. Also we per-formed both reactions in one-pot procedures.

Experimental

Organotin compounds were obtained by photostimulated reactions in liquid ammonia. Irradiation was conducted in a reactor equipped with two 250-W UV lamps emitting maximally at 350 nm. Cross coupling reactions were carried out with Pd(PPh3)2Cl2 as catalist (3-6%) and DMF as solvent.

Results and Discussion

The photostimulated reactions of Me3Sn- with dichloropyridines, di- and trichlorobenzenes afford di and tritin compounds in very goods yields:
Molecules 05 00431 i001
The palladium catalized cross coupling reactions of stannanes and aryl halides (PhBr or PhI) gave the respective arylated compounds:
Molecules 05 00431 i002
We also studied the possibility of performing the synthesis of the stannane and the Stille reaction in a one-pot procedure:
Molecules 05 00431 i003
All these results indicated that the SRN1 mechanism is an excellent method to obtain stannanes by the photostimulated reactions of mono-, di- and trichloro arenes with Me3Sn- in liquid ammonia. The stannanes thus obtained can be arylated by further reaction with bromo or iodoarenes through the pal-ladium catalyzed reactions (or to perform other palladium-catalyzed reactions). Further work is in pro-gress to examine reactions in a stepwise or one-pot conditions.

Acknowledgements 

This work was supported in part by CONICOR, FONCYT AND CONICET. E.C. gratefully acknowledges receipt a fellowship from Conicet.

References and Notes

  1. Rossi, R. A.; Pierini, A. B; Santiago, A. N. Aromatic Substitution by the SRN1 Reaction, Organic Reactions Vol. 54; Paquette, L. A., Bittman, R., Eds.; 1999; p. 1. [Google Scholar]
  2. Stille, J.K. Angew. Chem., Int. Ed. Engl. 1986, 25, 508. [CrossRef]
  3. Mitchell, T.N. Synthesis 1992, 803.
  4. Farina, V.; Krishnamurthy, V.; Scott, W.J. The Stille Reaction, Organic Reactions Vol. 50; Paquette, L. A., Ed.; 1997. [Google Scholar]

Share and Cite

MDPI and ACS Style

Corsico, E.F.; Rossi, R.A. SRN1 and Stille Reactions: A New Synthetic Strategy. Molecules 2000, 5, 431-432. https://doi.org/10.3390/50300431

AMA Style

Corsico EF, Rossi RA. SRN1 and Stille Reactions: A New Synthetic Strategy. Molecules. 2000; 5(3):431-432. https://doi.org/10.3390/50300431

Chicago/Turabian Style

Corsico, Eduardo F., and Roberto A. Rossi. 2000. "SRN1 and Stille Reactions: A New Synthetic Strategy" Molecules 5, no. 3: 431-432. https://doi.org/10.3390/50300431

Article Metrics

Back to TopTop