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worked in renamed species Dysphania, formerly Chenopodium
anorganic peroxides were already known.
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==History==
==History==
Ascaridole was the first and for a long time only discovered [[organic peroxide|peroxide]]. The structure was resolved by [[Otto Wallach]] in 1912,<ref name=Wal /> but the first synthesis was done by [[Karl Ziegler]] in 1944.<ref>{{cite journal
Ascaridole was the first and for a long time only discovered [[organic peroxide]]. The structure was resolved by [[Otto Wallach]] in 1912,<ref name=Wal /> but the first synthesis was done by [[Karl Ziegler]] in 1944.<ref>{{cite journal
| title = Die Synthese des Ascaridols
| title = Die Synthese des Ascaridols
| author = Günther, O. Schenck and K. Ziegler
| author = Günther, O. Schenck and K. Ziegler

Revision as of 06:02, 1 March 2009

Ascaridole
Ascaridole
Names
IUPAC names
1-methyl-4-(1-methylethyl)-2,3-
dioxabicyclo[2.2.2]oct-5-ene
Identifiers
ECHA InfoCard 100.007.408 Edit this at Wikidata
Properties
C10H16O2
Molar mass 168.23 g/mol
Density 1.0103 g/cm3
Melting point 3.3 °C
Boiling point 39-40 °C at 0.2 mmHg
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Ascaridole is a natural organic compound classified as a bicyclic monoterpene that has an unusual bridging peroxide functional group. It is the primary constituent of the oil of Mexican Tea (Dysphania ambrosioides, formerly Chenopodium ambrosioides).[1]

It is a colorless liquid that is soluble in most organic solvents. Like other low molecular weight organic peroxides, it is unstable and prone to explosion when heated or treated with organic acids.[2]

Ascaridole has been used as an anthelmintic for controlling nematodes.

History

Ascaridole was the first and for a long time only discovered organic peroxide. The structure was resolved by Otto Wallach in 1912,[2] but the first synthesis was done by Karl Ziegler in 1944.[3] The synthesis started from α-Terpinene which reacts with oxygen under the influence of chlorophyll and light. Under these conditions singlet oxygen is generated which is reacting in a Diels-Alder reaction with the dien system in the Terpinene.

References

  1. ^ Humphrey Paget (1938). "Chenopodium oil. Part III. Ascaridole". J. Chem. Soc. 392 (1): 829–833. doi:10.1039/JR9380000829.
  2. ^ a b O. Wallach (1912). "Zur Kenntnis der Terpene und der ätherischen Öle". Justus Liebig's Annalen der Chemie. 392 (1): 49–75. doi:10.1002/jlac.19123920104.
  3. ^ Günther, O. Schenck and K. Ziegler (1944). "Die Synthese des Ascaridols". Naturwissenschaften. 32 (14–26): 157. doi:10.1007/BF01467891.