An allylic rearrangement or allylic shift is an organic reaction in which reaction at a center vicinal to a double bond causes the double bond to shift to an adjacent pair of atoms:
It is encountered in both nucleophilic and electrophilic substitution, although it is usually Side reaction relative to non-allylic substitution. For example, reaction of 1-chloro-2-butene with sodium hydroxide gives 2-buten-1-ol and 3-buten-2-ol:
In the similar substitution of 1-chloro-3-methyl-2-butene, the secondary 2-methyl-3-buten-2-ol is produced in a yield of 85%, while that for the primary 3-methyl-2-buten-1-ol is 15%.
Allylic shifts occur because the transition state is an Allyl group intermediate. In other respects they are similar to classical nucleophilic substitution, and admit both bimolecular and monomolecular mechanisms (respectively the SN2' and SN1'/SNi' substitutions).
Scope
Allylic shifts become the dominant reaction pathway when there is substantial resistance to a normal (non-allylic) substitution. For nucleophilic substitution, such resistance is known when there is substantial steric hindrance at or around the
leaving group, or if there is a
geminal substituent destabilizing an accumulation of positive charge. The effects of substitution at the vinyl group are less clear.
that admit an
allyl complex also catalyze allylic substitution, sometimes to rates exceeding direct substitution.
Although rarer still than SN', allylic shifts can occur vinylogously, as a "butadienylic shift":[ Molecular yardsticks. Synthesis of extended equilibrium transfer alkylating cross-link reagents and their use in the formation of macrocycles Stephen J. Brocchini, Martin Eberle, and Richard G. Lawton J. Am. Chem. Soc.; 1988; 110(15) pp 5211 - 5212; ]
SN2' reduction
In
SN2' reduction, a
hydride allylically displaces a good
leaving group in a formal organic reduction, similar to the
Whiting reaction. One example occurred in taxol total synthesis (ring C):
[ Synthetic Studies on Taxol: Highly Stereoselective Construction of the Taxol C-Ring via SN2' Reduction of an Allylic Phosphonium Salt Masayuki Utsugi, Masayuki Miyano, and Masahisa Nakada Org. Lett.; 2006; 8(14) pp 2973 - 2976; (Letter) ]
The hydride is lithium aluminium hydride and the leaving group a phosphonium salt; the allylic shift causes the exocyclic double bond in the product. Only when the cyclohexane ring is properly substituted will the proton add trans isomer to the adjacent methyl group.
Electrophilic allyl shifts
Allyl shifts can also take place with
. In the example below the
carbonyl group in
benzaldehyde is activated by
diboronic acid prior to reaction with the allyl alcohol (see:
Prins reaction):
[ Highly Selective and Robust Palladium-Catalyzed Carbon-Carbon Coupling between Allyl Alcohols and Aldehydes via Transient Allylboronic Acids Nicklas Selander, Sara Sebelius, Cesar Estay, Kálmán J. Szabó European Journal of Organic Chemistry Volume 2006, Issue 18 , Pages 4085 - 4087 ]
The active catalyst system in this reaction is a combination of a
palladium pincer compound and
p-toluenesulfonic acid, the reaction product is obtained as a single
regioisomer and
stereoisomer.
Examples
Repeated allylic shifts can "flip-flop" a double-bond between two possible locations:
[ Double Lawton SN2' Addition to Epoxyvinyl Sulfones: Selective Construction of the Stereotetrads of Aplyronine A Ahmad El-Awa and Philip Fuchs Org. Lett.; 2006; 8(14) pp 2905 - 2908; (Letter) ]
An S
N2' reaction should explain the outcome of the reaction of an
aziridine carrying a methylene bromide group with
methyllithium:
[ Highly unusual conversion of 1-alkyl-2-(bromomethyl)aziridines into 1-alkyl-2-(N -alkyl-N -ethylaminomethyl)aziridines using methyllithium Matthias D'hooghe and Norbert De Kimpe Chem. Commun., 2007, 1275 - 1277, ]
In this reaction one equivalent of
acetylene is lost.
Named reactions
-
Ferrier rearrangement
-
Meyer–Schuster rearrangement
