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Truxillic acid

Truxillic acids are any of several crystalline stereoisomeric cyclic dicarboxylic acids with the formula (C6H5C2H2(CO2H)2. They are colorless solids. These compounds are obtained by the [2 + 2] photocycloadditions of cinnamic acid where the two trans alkenes react head-to-tail. The isolated stereoisomers are called truxillic acids.[1] The preparation of truxillic acids provided an early example of organic photochemistry.[2]

Truxillic acid
Names
IUPAC name
7,8′-Cyclo-8,7′-neolignane-9,9′-dioic acid
Systematic IUPAC name
2,4-Diphenylcyclobutane-1,3-dicarboxylic acid
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.022.478 Edit this at Wikidata
UNII
  • OC(C1C(C2=CC=CC=C2)C(C(O)=O)C1C3=CC=CC=C3)=O
Properties
C18H16O4
Molar mass 296.322 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Cinnamic Acid CycloAddition
Cinnamic Acid CycloAddition

Occurrence and reactions

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These compounds are found in a variety of plants, for example in coca.[3][4] Incarvillateine, an alkaloid from the plant Incarvillea sinensis, is a derivative of α-truxillic acid.

Upon heating, truxillic acids undergo cracking to give cinnamic acid.[5]

Isomers

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Truxillic acid can exist in five stereoisomers.[6][7]

 
Truxillic acid isomers
Isomer a b c d e f
α-truxillic acid
(cocaic acid[8])		 COOH H H C6H5 H COOH
γ-truxillic acid COOH H H C6H5 COOH H
ε-truxillic acid H COOH C6H5 H H COOH
peri-truxillic acid COOH H C6H5 H COOH H
epi-truxillic acid COOH H C6H5 H H COOH

Below are the five stereoisomers of truxillic acid, called alpha, gamma, epsilon, peri, and epi. These are shown both in a 2D skeletal diagram with stereocenters indicated and a 3D rendering of the structural geometry of the isomers themselves.

 
 

See also

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  • Truxinic acids are isomers of the truxillic acids with phenyl groups on adjacent methyne centers.

References

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  1. ^ Cohen, M. D.; Schmidt, G. M. J.; Sonntag, F. I. (1964). "Topochemistry. II. The photochemistry of trans-cinnamic acids". J. Chem. Soc.: 2000–2013. doi:10.1039/jr9640002000.
  2. ^ Roth, Heinz D. (1989). "The Beginnings of Organic Photochemistry". Angewandte Chemie International Edition in English. 28 (9): 1193–1207. doi:10.1002/anie.198911931.
  3. ^ Liebermann, C. (1888). "Ueber Cinnamylcocaïn". Berichte der Deutschen Chemischen Gesellschaft. 21 (2): 3372–3376. doi:10.1002/cber.188802102223.
  4. ^ Krauze-Baranowska, Miroslawa (2002). "Truxillic and truxinic acids-occurrence in plant kingdom". Acta Poliniae Pharmaceutica-Drug Research. 59 (5): 403–410. PMID 12602803.
  5. ^ Hein, Sara M. (2006). "An Exploration of a Photochemical Pericyclic Reaction Using NMR Data". Journal of Chemical Education. 83 (6): 940–942. Bibcode:2006JChEd..83..940H. doi:10.1021/ed083p940.
  6. ^ Stoermer, R.; Bachér, F. (1924). "Zur Stereoisomerie der Truxillsäuren und über die Auffindung der letzten Säure dieser Gruppe (VIII.)". Berichte der Deutschen Chemischen Gesellschaft (A and B Series). 57: 15–23. doi:10.1002/cber.19240570105.
  7. ^ Agarwai, O. P. (2011). Organic Chemistry Reactions and Reagents. Krishna Prakashan Media. ISBN 978-8187224655.
  8. ^ "ChemSpider ID 10218892". ChemSpider. Retrieved 15 October 2016.
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