Sarpong and Tantillo have examined the acid-catalyzed Prins/semipinacol rearrangement of hydroxylated pinenes, such as Reaction 1.1
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Rxn 1 |
Interestingly, only the fenchone scaffold products, like 1, are observed and the camphor scaffold products, like 2, are not observed. Cation intermediates are likely, and this means that a primary alkyl shift is taking place in preference to a tertiary alkyl shift, see Scheme 1.
Scheme 1.
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They proposed the following key steps in the reaction mechanism:
ωB97X-D/6-31+G(d,p) computations find a flat surface around cation intermediate 4: the TS leading to 5 and 6 are only 1.3 and 3.3 kcal mol-1, respectively. Since these small barriers are quite susceptible to changes in basis set and functional, and since Tantillo has found many examples of post-transition state bifurcations in cation systems, the authors reasonably decided to conduct molecular dynamics trajectories originating at the TS connecting 3 and 4. The geometries of the critical points are shown in Figure 1.
The trajectory study shows all the usual characteristics of reactions that are under dynamic control. A third of the trajectories show recrossing of the barrier, typical of very flat surfaces. Nearly all of the remaining trajectories led to 5, with only 2 trajectories (~1%) leading to 6. The dynamics are understandable in terms of favoring the primary alkyl shift over the tertiary since a significantly smaller mass needs to move in the former case.
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Figure 1. ωB97X-D/6-31+G(d,p) optimized geometries.
This is yet another study that implicates dynamic effects in routine reactions, one of many I have discussed over the years.
References
1. Blümel, M.; Nagasawa, S.; Blackford, K.; Hare, S. R.; Tantillo, D. J.; Sarpong, R., "Rearrangement of Hydroxylated Pinene Derivatives to Fenchone-Type Frameworks: Computational Evidence for Dynamically-Controlled Selectivity." J. Am. Chem. Soc. 2018, 140, 9291-9298, DOI: 10.1021/jacs.8b05804.
InChIs
1: InChI=1S/C17H20O2/c1-16-9-12-8-13(16)14(11-6-4-3-5-7-11)19-10-17(12,2)15(16)18/h3-7,12-14H,8-10H2,1-2H3/t12?,13?,14-,16?,17?/m0/s1
InChIKey=LTTUIPPXEHHMJS-XWTIBIIYSA-N
2: InChI=1S/C17H20O2/c1-16-10-19-15(11-6-4-3-5-7-11)13-8-12(16)9-14(18)17(13,16)2/h3-7,12-13,15H,8-10H2,1-2H3/t12?,13?,15-,16?,17?/m0/s1
InChIKey=GCKIOHNLJYVWKL-CMESGNGWSA-N
from Computational Organic Chemistry https://ift.tt/2wYeDLK
Sarpong and Tantillo have examined the acid-catalyzed Prins/semipinacol rearrangement of hydroxylated pinenes, such as Reaction 1.1
|
|
Rxn 1 |
Interestingly, only the fenchone scaffold products, like 1, are observed and the camphor scaffold products, like 2, are not observed. Cation intermediates are likely, and this means that a primary alkyl shift is taking place in preference to a tertiary alkyl shift, see Scheme 1.
Scheme 1.
|
|
|
They proposed the following key steps in the reaction mechanism:
ωB97X-D/6-31+G(d,p) computations find a flat surface around cation intermediate 4: the TS leading to 5 and 6 are only 1.3 and 3.3 kcal mol-1, respectively. Since these small barriers are quite susceptible to changes in basis set and functional, and since Tantillo has found many examples of post-transition state bifurcations in cation systems, the authors reasonably decided to conduct molecular dynamics trajectories originating at the TS connecting 3 and 4. The geometries of the critical points are shown in Figure 1.
The trajectory study shows all the usual characteristics of reactions that are under dynamic control. A third of the trajectories show recrossing of the barrier, typical of very flat surfaces. Nearly all of the remaining trajectories led to 5, with only 2 trajectories (~1%) leading to 6. The dynamics are understandable in terms of favoring the primary alkyl shift over the tertiary since a significantly smaller mass needs to move in the former case.
|
|
|
|
|
|
|
|
|
Figure 1. ωB97X-D/6-31+G(d,p) optimized geometries.
This is yet another study that implicates dynamic effects in routine reactions, one of many I have discussed over the years.
References
1. Blümel, M.; Nagasawa, S.; Blackford, K.; Hare, S. R.; Tantillo, D. J.; Sarpong, R., "Rearrangement of Hydroxylated Pinene Derivatives to Fenchone-Type Frameworks: Computational Evidence for Dynamically-Controlled Selectivity." J. Am. Chem. Soc. 2018, 140, 9291-9298, DOI: 10.1021/jacs.8b05804.
InChIs
1: InChI=1S/C17H20O2/c1-16-9-12-8-13(16)14(11-6-4-3-5-7-11)19-10-17(12,2)15(16)18/h3-7,12-14H,8-10H2,1-2H3/t12?,13?,14-,16?,17?/m0/s1
InChIKey=LTTUIPPXEHHMJS-XWTIBIIYSA-N
2: InChI=1S/C17H20O2/c1-16-10-19-15(11-6-4-3-5-7-11)13-8-12(16)9-14(18)17(13,16)2/h3-7,12-13,15H,8-10H2,1-2H3/t12?,13?,15-,16?,17?/m0/s1
InChIKey=GCKIOHNLJYVWKL-CMESGNGWSA-N
from Computational Organic Chemistry https://ift.tt/2wYeDLK
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