Cyclopropylacetylene

Cyclopropylacetylene
Names
	Preferred IUPAC name Ethynylcyclopropane
Identifiers
CAS Number	6746-94-7;
3D model (JSmol)	Interactive image;
ChemSpider	122425;
ECHA InfoCard	100.102.389
EC Number	425-430-1;
PubChem CID	138823;
CompTox Dashboard (EPA)	DTXSID80217795 ;
	InChI InChI=1S/C5H6/c1-2-5-3-4-5/h1,5H,3-4H2 Key: NPTDXPDGUHAFKC-UHFFFAOYSA-N;
	SMILES C#CC1CC1;
Properties
Chemical formula	C5H6
Molar mass	66.103 g·mol−1
Appearance	colorless liquid
Density	0.781 g/cm3 at 25°C
Boiling point	51–53 °C (124–127 °F; 324–326 K)
Hazards
	GHS labelling:
Pictograms
Hazard statements	H225, H315, H319, H412
Precautionary statements	P210, P273, P280, P305+P351+P338
Flash point	−17 °C (1 °F; 256 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

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

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:

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]

Synthesis scheme 2

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

^ "Cyclopropylacetylene : density 0.781 g/mL at 25 °C". Sigmaaldrich.com. Retrieved 26 April 2022.
^ "CYCLOPROPYL ACETYLENE". chemicalland21.com. Retrieved 31 May 2017.
^ Hudson, C.E.; Bauld, N.L. (1972). "Quantitative analysis of cyclopropyl β hyperfine splittings". J. Am. Chem. Soc. 94 (4): 1158. doi:10.1021/ja00759a021.
^ ^a ^b Corley, Edward G.; Thompson, Andrew S.; Huntington, Martha (2000). "CYCLOPROPYLACETYLENE". Organic Syntheses. 77. orgsyn.org: 231. doi:10.15227/orgsyn.077.0231. Retrieved 31 May 2017.

[1] "Cyclopropylacetylene : density 0.781 g/mL at 25 °C". Sigmaaldrich.com. Retrieved 26 April 2022.

[2] "CYCLOPROPYL ACETYLENE". chemicalland21.com. Retrieved 31 May 2017.

[3] Hudson, C.E.; Bauld, N.L. (1972). "Quantitative analysis of cyclopropyl β hyperfine splittings". J. Am. Chem. Soc. 94 (4): 1158. doi:10.1021/ja00759a021.

[orgsyn-4] Corley, Edward G.; Thompson, Andrew S.; Huntington, Martha (2000). "CYCLOPROPYLACETYLENE". Organic Syntheses. 77. orgsyn.org: 231. doi:10.15227/orgsyn.077.0231. Retrieved 31 May 2017.

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