Cyclobutanone
Names
Preferred IUPAC name
Cyclobutanone
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.013.405
UNII
  • InChI=1S/C4H6O/c5-4-2-1-3-4/h1-3H2
    Key: SHQSVMDWKBRBGB-UHFFFAOYSA-N
  • O=C1CCC1
Properties
C4H6O
Molar mass 70.091 g·mol−1
Appearance Colorless liquid
Density 0.9547 g/cm3 (0 °C)[1]
Melting point −50.9 °C (−59.6 °F; 222.2 K)[1]
Boiling point 99.75 °C (211.55 °F; 372.90 K)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Cyclobutanone is an organic compound with molecular formula (CH2)3CO. It is a four-membered cyclic ketone (cycloalkanone). It is a colorless volatile liquid at room temperature. Since cyclopropanone is highly sensitive, cyclobutanone is the smallest easily handled cyclic ketone.

Preparation

Kischner synthesized cyclobutanone from cyclobutanecarboxylic acid

The Russian chemist Nikolai Kischner first prepared cyclobutanone in a low yield from cyclobutanecarboxylic acid.[2][3] Kischner's process, involving several steps, is cumbersome and inefficient; more efficient, high-yielding syntheses have since been developed.[4]

One strategy involves degradation of five-carbon building blocks. For example, the oxidative decarboxylation of cyclobutanecarboxylic acid was improved by the use of other reagents and methods.

A newer, more efficient preparation of cyclobutanone was found by P. Lipp and R. Köster in which a solution of diazomethane in diethyl ether is reacted with ketene.[5] This reaction is based on a ring expansion of the cyclopropanone intermediate initially formed, wherein molecular nitrogen is split off:

The reaction mechanism was confirmed by a reaction using 14C-labeled diazomethane.[6]

Another synthesis of cyclobutanone involves lithium-catalyzed rearrangement of oxaspiropentane, which is formed by epoxidation of the easily accessible methylenecyclopropane:[7][8]

Cyclobutanone can also be prepared in a two step procedure by dialkylation of 1,3-dithiane with 1-bromo-3-chloropropane followed by deprotection to the ketone with mercuric chloride (HgCl2) and cadmium carbonate (CdCO3).[9]

Reactions

At about 350 °C, cyclobutanone decomposes into ethylene and ketene.[10] The activation energy for this [2+2] cycloelimination is 52 kcal/mol. The reverse reaction, the [2+2] cycloaddition of ketene and ethylene, has never been observed.

Decomposition of cyclobutanone

See also

Other cyclic ketones:

References

  1. 1 2 3 CRC Handbook of Chemistry and Physics. Vol. 90. Boca Raton, Florida: CRC Press.
  2. ↑ N. Kishner (1905). "'Über die Einwirkung von Brom auf die Amide α-bromsubstituierter Säuren". Journal der Russischen Physikalisch-Chemischen Gesellschaft. 37: 103–105.
  3. ↑ N. Kishner (1905). "Über das Cyklobutanon". Journal der Russischen Physikalisch-Chemischen Gesellschaft. 37: 106–109.
  4. ↑ Dieter Seebach (1971). "Isocyclische Vierringverbindungen". In Houben; Weyl; Müller (eds.). Methoden der Organischen Chemie. Vol. IV/4. Stuttgart: Georg Thieme Verlag.
  5. ↑ P. Lipp und R. Köster (1931). "Ein neuer Weg zum Cyclobutanon". Berichte der Deutschen Chemischen Gesellschaft. 64 (11): 2823–2825. doi:10.1002/cber.19310641112.
  6. ↑ Semenow, Dorothy A.; Cox, Eugene F.; Roberts, John D. (1956). "Small-Ring Compounds. XIV. Radioactive Cyclobutanone from Ketene and Diazomethane-14C1". Journal of the American Chemical Society. 78 (13): 3221–3223. doi:10.1021/ja01594a069.
  7. ↑ Salaün, J. R.; Conia, J. M. (1971). "Oxaspiropentane. A rapid route to cyclobutanone". Journal of the Chemical Society D: Chemical Communications (23): 1579b–1580. doi:10.1039/C2971001579B.
  8. ↑ J. R. Salaün, J. Champion, J. M. Conia (1977). "Cyclobutanone from Methylenecyclopropane via Oxaspiropentane". Organic Syntheses. 57: 36. doi:10.15227/orgsyn.057.0036.{{cite journal}}: CS1 maint: multiple names: authors list (link); Collective Volume, vol. 6, p. 320
  9. ↑ D. Seebach, A. K. Beck (1971). "Cyclic Ketones from 1,3-Dithiane: Cyclobutanone". Organic Syntheses. 51: 76. doi:10.15227/orgsyn.051.0076.; Collective Volume, vol. 6, p. 316
  10. ↑ Das, M. N.; Kern, F.; Coyle, T. D.; Walters, W. D. (1954). "The Thermal Decomposition of Cyclobutanone1". Journal of the American Chemical Society. 76 (24): 6271–6274. doi:10.1021/ja01653a013.
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