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All 3 posts Subject: While looking through old cannabinoid papers I Please login to post Down

Lilienthal
(Moderator)
12-03-03 21:03
No 474534
User Picture       While looking through old cannabinoid papers I

While looking through old cannabinoid papers I found this interesting transformation. Unfortunately I have only the first page...

Tet. Lett. 49 4841 - 4844 (1973) describes the quantitative conversion of 4-methoxy-cinnamic acid to a mixture of anethole (propen-1-yl-4-methoxybenzene) and estragole (1-allyl-4-methoxybenzene) with LiAlH4 / AlCl3 in ether.

lugh
(Moderator)
12-05-03 19:57
No 474847
      Request Retrieved
(Rated as: good read)

Here's the entire article wink

A One-step Ester to Hydrocarbon Reduction
Donald C. Wigfield and Kevser Taymaz
Tetrahedron Lett., 49, 4481-4484 (1973)

Chemistry is our Covalent Bond

Rhodium
(Chief Bee)
12-11-03 16:22
No 476162
User Picture       A One-Step Ester to Hydrocarbon Reduction
(Rated as: good read)

A One-Step Ester to Hydrocarbon Reduction
Donald C. Wigfield and Kevser Taymaz
Tetrahedron Letters 49, 4841-4844 (1973)

Oxidation and reduction constitute an important part of organic chemistry, and such reactions of oxygenated functional groups occupy a central place in this area, with many reactions having been developed to transform one functionality into another of differing oxidation level. The reduction of a Group III oxidation level¹ functional group (e.g. -COOR) to a Group 0 functional group (-CH₃) is, however, a transformation for which there is no general one-step reaction². Indeed, even the number of specific one-step transformations of this type that have been reported is rather small, the examples being apparently restricted to catalytic hydrogenation of certain substrates under vigorous conditions³.

In view of the dearth of such reactions, we wish to report a reaction that we have discovered in the course of other work. Ethyl p-methoxycinnamate 1, on reduction with LiAlH₄-AlCl₃ in ether, gives not the expected p-methoxycinnamyl alcohol, but a quantitative yield of the two isomers anethole 2 and p-allylanisole (estragole) 3 in a 2:1 ratio (glc ratio 66:34). The identity of these compounds was established chromatographically using authentic samples (6 foot, 5% QF-1 on Chromosorb G column at 1400, anethole retention time 10.5 min., p-allylanisole retention time 4.7 min.) followed by preparative glc (QF-1) purification and demonstration of identity of spectral properties with those of authentic samples.

This reaction is, thus, an extremely rare instance of a one-step reduction of an ester to the corresponding hydrocarbon initiated by a metal hydride reagent⁷. That it is by no means general, however, is immediately clear from the reduction of the closely related ethyl cinnamate, which has been reported to reduce normally to the primary alcohol under apparently identical conditions to ours⁸. To ensure that this abrupt difference in reaction was due to the methoxyl substituent and was not an artifact of the comparison of results from different laboratories, ethylcinnamate was reduced, giving no hydrocarbon and producing cinnamyl alcohol in 95% yield, confirming the result of Jorgenson⁸. Although at first sight the effect of methoxyl might be surprising since hydride reductions of ketones are known to show positive p values^9-11 presumably the reduction to the hydrocarbon involves Lewis acid-catalyzed¹² carbonium ion formation with a substantial negative p value.

In a search of the literature to find closely related reactions we have found reports of certain alcohols being reduced to hydrocarbons under LiAlH₄-AlCl₃ conditions^13,14, and in a particularly relevant paper, the reductions of p-amino- and p-methoxybenzaldehydes to the corresponding toluenes, the electron donating substituents being essential for reduction to the hydrocarbon¹⁵. Thus although the reaction at hand may at present be almost unique, its existence might not have been entirely unpredictable, the possibly surprising feature being the quantitative ester reduction accompanied by no detectable double bond reduction.

In order to explore the limited generality of the reaction, reduction of the corresponding aldehyde and alcohol were also studied. p-Methoxycinnamyl alcohol, produced by LiAlH₄ reduction of methyl p-methoxycinnamate¹⁶, also was reduced by LiAlH₄-AlCl₃ giving a quantitative yield of the anethole-estragole mixture in essentially the same proportions (64:36). p-Methoxycinnamaldehyde, produced by MnO₂ oxidation of p-methoxycinnamyl alcohol¹⁶, was also reduced quantitatively to give the same hydrocarbon mixture (anethole:estragole 67:33).

Reduction of ethyl o-methoxycinnamate also gave quantitative reduction to hydrocarbon, the proportion of double bond isomers, however, being slightly different (o-anethole 56%, o-Estragole 44%).

The reduction in a system with an amino activating group, rather than methoxyl was also attempted. Reduction of ethyl p-aminocinnamate under the same conditions gave a complex mixture of products, from which the corresponding hydrocarbons p-allylaniline and p-propenylaniline¹⁷ could be extracted only with tedious purification and in 18% yield.

References and Footnotes

1. J. B. Hendrickson, D. J. Cram, and G. S. Hammond, Organic Chemistry. McGraw-Hill Book Company Inc., New York. 3rd Edition, 1970, p. 74.
2. Clearly there are many ways of accomplishing this transformation in more than one step.
3. P. N. Rylander. Catalytic hydrogenation over platinum metals. Academic Press, New York, 1967, pp. 230, 320, 476.
4. T. W. Campbell, S. Linden, S. Godshalk, and W. G. Young, J. Amer. Chem. Soc., 69, 880 (1947).
5. E. A. Braude, J. Chem. Soc., 1902 (1949).
6. A. E. Lutskii, A. F. Soldatova and E. M. Voroshin, Zh. Obshch. Khim., 35, 2099 (1965).
7. For another example, see H. O. House, Modern Synthetic Reactions. W. A. Benjamin, Inc., Menlo Park, California, 1972, p. 84.
8. M. J. Jorgenson, Tetrahedron Letters, 559 (1962).
9. J. A. Parry and K. D. Warren, J. Chem. Soc., 4049 (1965). 10. K. Bowden and M. Hardy, Tetrahedron, 22, 1169 (1966).
11. A. F. Cockerill and D. M. Rackham, J. Chem. Soc., Perkin II, 2076 (1972).
12. In this mixture, several species are possible, see U. E. Diner, H. A. Davis, and R. K. Brown, Can. J. Chem., 45, 207 (1967).
13. J. H. Brewster, S. F. Osman, H. O. Bayer, and H. B. Hopps, J. Org. Chem., 29, 121 (1964).
14. S. B. Nerali and K. K. Chakravarti, Tetrahedron Letters, 2447 (1967).
15. B. R. Brown and A. M. S. White, J. Chem. Soc., 3755 (1957).
16. D. Marshall and M. C. Whiting, J. Chem. Soc., 4082 (1956).
17. C. D. Hund and W. W. Jenkins, J. Org. Chem., 22, 1418 (1957).

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	All 3 posts		Subject: While looking through old cannabinoid papers I		Please login to post		Down


		Lilienthal (Moderator) 12-03-03 21:03 No 474534				While looking through old cannabinoid papers I
						While looking through old cannabinoid papers I found this interesting transformation. Unfortunately I have only the first page... Tet. Lett. 49 4841 - 4844 (1973) describes the quantitative conversion of 4-methoxy-cinnamic acid to a mixture of anethole (propen-1-yl-4-methoxybenzene) and estragole (1-allyl-4-methoxybenzene) with LiAlH4 / AlCl3 in ether.



		lugh (Moderator) 12-05-03 19:57 No 474847				Request Retrieved (Rated as: good read)
						Here's the entire article A One-step Ester to Hydrocarbon Reduction Donald C. Wigfield and Kevser Taymaz Tetrahedron Lett., 49, 4481-4484 (1973) Chemistry is our Covalent Bond



		Rhodium (Chief Bee) 12-11-03 16:22 No 476162				A One-Step Ester to Hydrocarbon Reduction (Rated as: good read)
						A One-Step Ester to Hydrocarbon Reduction Donald C. Wigfield and Kevser Taymaz Tetrahedron Letters 49, 4841-4844 (1973) Oxidation and reduction constitute an important part of organic chemistry, and such reactions of oxygenated functional groups occupy a central place in this area, with many reactions having been developed to transform one functionality into another of differing oxidation level. The reduction of a Group III oxidation level¹ functional group (e.g. -COOR) to a Group 0 functional group (-CH₃) is, however, a transformation for which there is no general one-step reaction². Indeed, even the number of specific one-step transformations of this type that have been reported is rather small, the examples being apparently restricted to catalytic hydrogenation of certain substrates under vigorous conditions³. In view of the dearth of such reactions, we wish to report a reaction that we have discovered in the course of other work. Ethyl p-methoxycinnamate 1, on reduction with LiAlH₄-AlCl₃ in ether, gives not the expected p-methoxycinnamyl alcohol, but a quantitative yield of the two isomers anethole 2 and p-allylanisole (estragole) 3 in a 2:1 ratio (glc ratio 66:34). The identity of these compounds was established chromatographically using authentic samples (6 foot, 5% QF-1 on Chromosorb G column at 1400, anethole retention time 10.5 min., p-allylanisole retention time 4.7 min.) followed by preparative glc (QF-1) purification and demonstration of identity of spectral properties with those of authentic samples. This reaction is, thus, an extremely rare instance of a one-step reduction of an ester to the corresponding hydrocarbon initiated by a metal hydride reagent⁷. That it is by no means general, however, is immediately clear from the reduction of the closely related ethyl cinnamate, which has been reported to reduce normally to the primary alcohol under apparently identical conditions to ours⁸. To ensure that this abrupt difference in reaction was due to the methoxyl substituent and was not an artifact of the comparison of results from different laboratories, ethylcinnamate was reduced, giving no hydrocarbon and producing cinnamyl alcohol in 95% yield, confirming the result of Jorgenson⁸. Although at first sight the effect of methoxyl might be surprising since hydride reductions of ketones are known to show positive p values^9-11 presumably the reduction to the hydrocarbon involves Lewis acid-catalyzed¹² carbonium ion formation with a substantial negative p value. In a search of the literature to find closely related reactions we have found reports of certain alcohols being reduced to hydrocarbons under LiAlH₄-AlCl₃ conditions^13,14, and in a particularly relevant paper, the reductions of p-amino- and p-methoxybenzaldehydes to the corresponding toluenes, the electron donating substituents being essential for reduction to the hydrocarbon¹⁵. Thus although the reaction at hand may at present be almost unique, its existence might not have been entirely unpredictable, the possibly surprising feature being the quantitative ester reduction accompanied by no detectable double bond reduction. In order to explore the limited generality of the reaction, reduction of the corresponding aldehyde and alcohol were also studied. p-Methoxycinnamyl alcohol, produced by LiAlH₄ reduction of methyl p-methoxycinnamate¹⁶, also was reduced by LiAlH₄-AlCl₃ giving a quantitative yield of the anethole-estragole mixture in essentially the same proportions (64:36). p-Methoxycinnamaldehyde, produced by MnO₂ oxidation of p-methoxycinnamyl alcohol¹⁶, was also reduced quantitatively to give the same hydrocarbon mixture (anethole:estragole 67:33). Reduction of ethyl o-methoxycinnamate also gave quantitative reduction to hydrocarbon, the proportion of double bond isomers, however, being slightly different (o-anethole 56%, o-Estragole 44%). The reduction in a system with an amino activating group, rather than methoxyl was also attempted. Reduction of ethyl p-aminocinnamate under the same conditions gave a complex mixture of products, from which the corresponding hydrocarbons p-allylaniline and p-propenylaniline¹⁷ could be extracted only with tedious purification and in 18% yield. References and Footnotes 1. J. B. Hendrickson, D. J. Cram, and G. S. Hammond, Organic Chemistry. McGraw-Hill Book Company Inc., New York. 3rd Edition, 1970, p. 74. 2. Clearly there are many ways of accomplishing this transformation in more than one step. 3. P. N. Rylander. Catalytic hydrogenation over platinum metals. Academic Press, New York, 1967, pp. 230, 320, 476. 4. T. W. Campbell, S. Linden, S. Godshalk, and W. G. Young, J. Amer. Chem. Soc., 69, 880 (1947). 5. E. A. Braude, J. Chem. Soc., 1902 (1949). 6. A. E. Lutskii, A. F. Soldatova and E. M. Voroshin, Zh. Obshch. Khim., 35, 2099 (1965). 7. For another example, see H. O. House, Modern Synthetic Reactions. W. A. Benjamin, Inc., Menlo Park, California, 1972, p. 84. 8. M. J. Jorgenson, Tetrahedron Letters, 559 (1962). 9. J. A. Parry and K. D. Warren, J. Chem. Soc., 4049 (1965). 10. K. Bowden and M. Hardy, Tetrahedron, 22, 1169 (1966). 11. A. F. Cockerill and D. M. Rackham, J. Chem. Soc., Perkin II, 2076 (1972). 12. In this mixture, several species are possible, see U. E. Diner, H. A. Davis, and R. K. Brown, Can. J. Chem., 45, 207 (1967). 13. J. H. Brewster, S. F. Osman, H. O. Bayer, and H. B. Hopps, J. Org. Chem., 29, 121 (1964). 14. S. B. Nerali and K. K. Chakravarti, Tetrahedron Letters, 2447 (1967). 15. B. R. Brown and A. M. S. White, J. Chem. Soc., 3755 (1957). 16. D. Marshall and M. C. Whiting, J. Chem. Soc., 4082 (1956). 17. C. D. Hund and W. W. Jenkins, J. Org. Chem., 22, 1418 (1957). The Hive - Clandestine Chemists Without Borders

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