Barrelene

The original Zimmerman synthesis modified in 1969{{Cite journal |last=Zimmerman |first=Howard E. |last2=Grunewald |first2=Gary L. |last3=Paufler |first3=Robert M. |last4=Sherwin |first4=Maynard A. |date=April 1969 |title=Synthesis and physical properties of barrelene, a unique Moebius-like molecule |url=https://pubs.acs.org/doi/abs/10.1021/ja01037a024 |journal=Journal of the American Chemical Society |language=en |volume=91 |issue=9 |pages=2330–2338 |doi=10.1021/ja01037a024 |issn=0002-7863|url-access=subscription }} starts from coumalic acid:Reaction scheme: decarboxylation of coumalic acid (1) takes place at 650 °C with copper to give α-pyrone (2). The reaction with methyl vinyl ketone (3) is a tandem Diels–Alder/retro-Diels–Alder/Diels–Alder sequence, which yields di-ketone 5 as a mixture of two isomers. It is possible to convert the endo isomer 5b to the exo isomer 5a by an epimerization process through the enol. The ketone groups are converted to oxime groups in 6 by reaction with hydroxylamine and then to the tosylate groups in 7 by reaction with tosyl chloride. A basic Beckmann rearrangement takes the scheme to give amide 8 and its hydrolysis to the di-amine 9 takes place with sodium hydroxide. Finally, a Hofmann elimination through ammonium salt 10 gives the barrelene 11.

:File:Synthesis of barrelene.svg{{clear-left}}

Many alternative routes have been devised since then, one of them starting from benzene oxide:{{Cite journal |last=Cossu |first=Sergio |last2=Battaggia |first2=Simone |last3=De Lucchi |first3=Ottorino |date=1997-06-13 |title=Barrelene, a New Convenient Synthesis |url=https://pubs.acs.org/doi/10.1021/jo962267f |journal=The Journal of Organic Chemistry |language=en |volume=62 |issue=12 |pages=4162–4163 |doi=10.1021/jo962267f |issn=0022-3263|url-access=subscription }}Step one in this reaction between oxepin (one of the possible tautomers) with (Z)-1,2-bis(phenylsulfonyl)ethylene is a Diels–Alder reaction. The reagents for de-epoxidation are tungsten hexachloride and butyllithium. The second elimination reaction takes place with sodium amalgam in Julia olefination style.

:File:Cossu synthesis of barrelene.svg

An alternate route that allows synthesis of the parent barrelene system and a variety of substituted barrelenes has also been reported.{{Cite journal |last=Wagaman |first=Michael W. |last2=Bellmann |first2=Erika |last3=Cucullu |first3=Michèle |last4=Grubbs |first4=Robert H. |date=1997-12-01 |title=Synthesis of Substituted Bicyclo[2.2.2]octatrienes |url=https://pubs.acs.org/doi/10.1021/jo971039y |journal=The Journal of Organic Chemistry |language=en |volume=62 |issue=26 |pages=9076–9082 |doi=10.1021/jo971039y |issn=0022-3263}}

Image:Barrelene - 2.png

Barrelene is hydrogenated with hydrogen gas and Adams' catalyst in ethanol to the fully saturated bicyclo[2.2.2]-octane. Bromination with bromine in tetrachloromethane gives a di-bromo adduct because a coupling reaction intervenes:

:Image:BarreleneBromination.png

Epoxidation of barrelene with oxone gives the trioxatrishomobarreleneendo, exo,syn-3,7,10-Trioxapentacyclo[3.3.3.0^2,4.0^6,8.0^9,11]undecane which on rearrangement with boron trifluoride (driving force:relief of strain energy) converts into the trioxatrishomocubane:{{Cite journal |last=Kozhushkov |first=Sergei I. |last2=Preuß |first2=Thomas |last3=Yufit |first3=Dmitrii S. |last4=Howard |first4=Judith A. K. |last5=Meindl |first5=Kathrin |last6=Rühl |first6=Stephan |last7=Yamamoto |first7=Chiyo |last8=Okamoto |first8=Yoshio |last9=Schreiner |first9=Peter R. |last10=Rinderspacher |first10=B. Christopher |last11=de Meijere |first11=Armin |date=June 2006 |title=4,7,11‐Triheterotrishomocubanes – Propeller‐Shaped Highly Symmetrical Chiral Molecules Derived from Barrelene |url=https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.200600019 |journal=European Journal of Organic Chemistry |language=en |volume=2006 |issue=11 |pages=2590–2600 |doi=10.1002/ejoc.200600019 |issn=1434-193X|url-access=subscription }}

:Image:TrioxatrishomocubaneSynthesis.png

This compound can be envisioned as a cubane with three oxygen atoms inserted into three opposite edges or as 9-crown-3 capped by two methine units. The molecule is chiral and the separate enantiomers have been isolated.

Certain barrelenes have been used as a monomer in a ring opening metathesis polymerization:{{Cite journal |last=Pu |first=Lin |last2=Wagaman |first2=Michael W. |last3=Grubbs |first3=Robert H. |date=1996-01-01 |title=Synthesis of Poly(1,4-naphthylenevinylenes): Metathesis Polymerization of Benzobarrelenes |url=https://pubs.acs.org/doi/10.1021/ma9500143 |journal=Macromolecules |language=en |volume=29 |issue=4 |pages=1138–1143 |doi=10.1021/ma9500143 |issn=0024-9297|url-access=subscription }}{{Cite journal |last=Wagaman |first=Michael W. |last2=Grubbs |first2=Robert H. |date=1997-07-01 |title=Synthesis of Organic and Water Soluble Poly(1,4-phenylenevinylenes) Containing Carboxyl Groups: Living Ring-Opening Metathesis Polymerization (ROMP) of 2,3-Dicarboxybarrelenes |url=https://pubs.acs.org/doi/10.1021/ma9701595 |journal=Macromolecules |language=en |volume=30 |issue=14 |pages=3978–3985 |doi=10.1021/ma9701595 |issn=0024-9297|url-access=subscription }}

:Image:BarrelenePolymerization.png

The catalyst is a Schrock carbene (a molybdenum bis-(hexafluoro-tert-butoxy) carbene catalyst) and the long alkyl chain attached to the monomer is required for solubility. Oxidation of the polymer with DDQ affords the naphthalene pendant of poly(p-phenylene vinylene).

Isopentane solutions of barrelene undergo photolytic isomerisation when acetone is added as a photosensitizer to produce semibullvalene. Prolonged irradiation results in further isomerisation to form cyclooctatetraene.

{{cite journal |doi= 10.1021/ja00953a045 |last1= Zimmerman|first1= H. E.|last2= Grunewald|first2= G. L.|year= 1966|title= The Chemistry of Barrelene. III. A Unique Photoisomerization to Semibullvalene|journal= J. Am. Chem. Soc.|volume= 88|issue= 1|pages= 183–184}}

:Image:Semibullvalene_synthesis.svg

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Category:Cycloalkenes

Category:Bicyclic compounds