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22 March 2000

Stereoselective Synthesis of 8-Trialkylstannylmenthols

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Instituto de Investigaciones en Química Orgánica, Departamento de Química e Ing.Qca., Universidad Nacional del Sur, Av. Alem 1253, 8000 Bahía Blanca, Argentina
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Abstract

Trialkyltin menthones of type 2 are obtained selectively by 1,4-addition of trialkylstannyl lithium to (-)-pulegone. Reduction of 2 with borane in THF using as catalyst the reagent prepared from borane and (S)-valinol gave a mixture of the corresponding trialkyltin alcohols 3 (Me: 84%; n-Bu: 90,6%) and 4 (Me: 16% and n-Bu: 9,4%).

Introduction

Taking into account the excellent results obtained with the (-)-8-phenylmenthyl group as a chiral auxiliary, we considered of interest the synthesis of some organotin analogues. The 8-triorganotinmenthyl moiety might affect the stereoselectivity due to its bulk and also to electronic effects. The stereoselective synthesis of these compounds was carried out according to Scheme 1 and Scheme 2.
Scheme 1. 1,4-Addition of trialkylstannyl lithium to (-)-pulegone.
Scheme 2. Stereoselective reduction of trialkylstannylmenthones of type 2.

Experimental

The 1,4-addition of trimethyl- and tri-n-butyl lithium to (-)-pulegone led to menthones of type 1 and 2 with an average yield of 72% following standard techniques [1]. Compounds 1 and 2 were separated by column chromatography (silica gel 60). The reduction of type 2 ketones with borane in THF using (S)-valinol as a catalyst was carried out according to known procedures [2].

Results and Discussion

The reduction of (-)-menthone carried out with the reagent prepared from borane and (S)-valinol in THF in order to determine the degree of asymmetric induction which can be achieved with this reagent, yielded quantitatively a mixture of (-)-menthol (80%) and (+)-neo-menthol (20%), i.e., 60% of diastereoisomeric excess (d.e.).
Under the same reaction conditions, the reduction of 2a (d.e. 68%) and 2b (d.e. 81,3%) led to the corresponding 8-trialkylstannylmenthols with better diastereoisomeric excesses.

Acknowledgements:

This work was supported by CONICET (Buenos Aires), CIC (Provincia de Buenos Aires) and Universidad Nacional del Sur (Bahía Blanca, Argentina).

References and Notes

  1. Radivoy, G.E. Doctor in Chemistry Thesis, Universidad Nacional del Sur, 1997.
  2. Itsuno, S.; Nakano, M.; Miyazaky, K; Masuda, H.; Ito, K.; Hirao, A; Nakahama, S. Asymmetric Synthesis Using Chirally Modified Borohydrides. Part 3. Enantioselective Reduction of Ketones and Oxime Ethers with Reagents Prepared from Borane and Chiral Amino Alcohols. J. Chem. Soc. Perkin Trans. I 1985, 2039. [Google Scholar] [CrossRef]

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