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Cyclopropylacetylene

Chemical compound From Wikipedia, the free encyclopedia

Cyclopropylacetylene
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Cyclopropylacetylene is an hydrocarbon with the chemical formula C
5
H
6
.[2] Under normal conditions, the substance is a colorless liquid. Cyclopropylacetylene is a precursor to pharmaceuticals and other organic compounds.

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Synthesis

Several methods have been published on the synthesis of cyclopropylacetylene. The earliest preparation starts with the chlorination of cyclopropylmethylketone with phosphorus pentachloride.[3] Thereafter, the reaction product, 1-cyclopropyl-1,1-dichloroethane, is converted into cyclopropylacetylene via double dehydrochlorination. This occurs in presence of a strongly basic solution, such as potassium tert-butoxide in dimethyl sulfoxide:

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Synthesis scheme 1

However, the yield of this method is not substantial (20-25%).[4] A one-pot synthesis of cyclopropylacetylene has been reported in which 5-chloro-1-pentyne reacts with n-butyl lithium or n-hexyl lithium. Cyclohexane is used as a solvent. The reaction is a metalation followed by a cyclization. The reaction product is then cooled, and an aqueous solution of ammonium chloride is added slowly. There is a two-phase mixture: a heavy water phase and a lighter organic phase containing cyclopropylacetylene.[4]

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Synthesis scheme 2
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Applications

Cyclopropylacetylene is used as reagent in organic reactions. It is, for example, a building block of the antiretroviral and psychotropic drug efavirenz. It can also be used in the azide-alkyne Huisgen cycloaddition.

References

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