Chemistry:Cyclopentenone
| |||
| Names | |||
|---|---|---|---|
| Preferred IUPAC name
Cyclopent-2-en-1-one | |||
| Identifiers | |||
3D model (JSmol)
|
|||
| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
PubChem CID
|
|||
| UNII | |||
| |||
| |||
| Properties | |||
| C5H6O | |||
| Molar mass | 82.102 g·mol−1 | ||
| Density | 0.98 g·mL−1 | ||
| Boiling point | 150 °C (302 °F; 423 K) | ||
| almost insoluble in water | |||
| Hazards | |||
| Main hazards | Harmful | ||
| Flash point | 42 °C (108 °F; 315 K) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
 verify (what is   ?)
| |||
| Infobox references | |||
2-Cyclopentenone is the organic compound with the chemical formula (CH
2)
2(CH)
2CO. 2-Cyclopentenone contains two functional groups, a ketone and an alkene. It is a colorless liquid. Its isomer, 3-cyclopentenone is less commonly encountered.
The term cyclopentenone may also refer to a structural motif wherein the cyclopentenone moiety is a subunit of a larger molecule. Cyclopentenones are found in a large number of natural products, including jasmone, the aflatoxins, and several prostaglandins.[1]
Synthesis
2-Cyclopentenones can be synthesized in a number of ways. One of the routes involves elimination of α-bromo-cyclopentanone using lithium carbonate[2] and Claisen condensation-decarboxylation-isomerization cascades of unsaturated diesters as shown below.[3]
The acid-catalyzed dehydration of cyclopentanediols affords cyclopentenone.[4]
As a functional group, the synthesis of 2-cyclopentenones is accomplished in a variety of other ways, including the Nazarov cyclization reaction from divinyl ketones, Saegusa–Ito oxidation from cyclopentanones, ring-closing metathesis from the corresponding dienes, oxidation of the corresponding cyclic allylic alcohols, and the Pauson–Khand reaction from alkenes, alkynes, and carbon monoxide.[5]
Reactions
As an enone, 2-cyclopentenone undergoes the typical reactions of α-β unsaturated ketones, including nucleophilic conjugate addition, the Baylis–Hillman reaction, and the Michael reaction. Cyclopentenone also functions as an excellent dienophile in the Diels–Alder reaction, reacting with a wide variety of dienes. In one example, a Danishefsky-type diene is reacted with a cyclopentenone to yield a fused tricyclic system en route to the synthesis of coriolin.[6]
Occurrence
It has been isolated from pressure-cooked pork liver by simultaneous steam distillation and continuous solvent extraction.[7][8]
Related compounds
- cyclopropenone
- cyclobutenone[9]
- cyclohexenone
- cycloheptenone[10]
References
- ↑ Simeonov, Svilen P.; Nunes, João P. M.; Guerra, Krassimira; Kurteva, Vanya B.; Afonso, Carlos A. M. (2016-05-25). "Synthesis of Chiral Cyclopentenones" (in en). Chemical Reviews 116 (10): 5744–5893. doi:10.1021/cr500504w. ISSN 0009-2665. PMID 27101336. https://pubs.acs.org/doi/10.1021/cr500504w.
- ↑ Daisuke, Fukushima & Hirata Norihiko, "Process for producing 2-bromocyclopentanone", US patent EP1418166, published 2004-05-12
- ↑ Liang, Shelue; Andrea Haunert & Sylvia Huber-Dirr et al., "Process for preparing cyclopentenone", US patent EP1422212, published 2004-11-25
- ↑ Charles H. DePuy; K. L. Eilers (1962). "2-Cyclopentenone". Org. Synth. 42: 38. doi:10.15227/orgsyn.042.0038.
- ↑ Müller, Reto. "Synthesis of cyclopentenones". https://www.organic-chemistry.org/synthesis/C1C/cyclic/enones/cyclopentenones.shtm.
- ↑ Danishefsky, Samuel; Zamboni, Robert; Kahn, Michael; Etheredge, Sarah Jane (March 1980). "Total synthesis of dl-coriolin". Journal of the American Chemical Society 102 (6): 2097–2098. doi:10.1021/ja00526a061.
- ↑ Mussinan, Cynthia J.; Walradt, John P. (May 1974). "Volatile constituents of pressure cooked pork liver". Journal of Agricultural and Food Chemistry 22 (5): 827–831. doi:10.1021/jf60195a002.
- ↑ Simeonov, Svilen P.; Nunes, João P. M.; Guerra, Krassimira; Kurteva, Vanya B.; Afonso, Carlos A. M. (2016). "Synthesis of Chiral Cyclopentenones". Chemical Reviews 116 (10): 5744–5893. doi:10.1021/cr500504w. PMID 27101336.
- ↑ A. G. Ross, X. Li, S. J. Danishefsky (2012). "Preparation of Cyclobutenone". Organic Syntheses 89: 491. doi:10.15227/orgsyn.089.0491.
- ↑ Y. Ito, S. Fujii, M. Nakatuska, F. Kawamoto,T. Saegusa (1979). "One-Carbon Ring Expansion of Cycloalkanones to Conjugated Cycloalkenones: 2-Cyclohepten-1-One". Organic Syntheses 59: 113. doi:10.15227/orgsyn.059.0113.
 |  |
