Cymene
Cymene describes organic compounds with the formula CH3C6H4CH(CH3)2. Three isomers exist: 1,2- 1,3-, and 1,4-. All are colorless liquids, immiscible in water, with similar boiling points. They are classified are aromatic hydrocarbons. The bearing two substituents: an isopropyl (CH(CH3)2) group and a methyl group.[1]
| Cymenes | |||
| Name | o-Cymene | m-Cymene | p-Cymene |
|---|---|---|---|
| Structural formula |  |  |  |
| CAS number | 527-84-4 | 535-77-3 | 99-87-6 |
| melting point | -71.54 | -63.75 | -67.94 |
| boiling point (°C) | 178.15 | 175.05 | 177.10 |
Production and reactions
m- and p-Cymene are prepared by alkylation of toluene with propylene:
- CH3C6H5 + 2 CH3CH=CH2 → CH3C6H4CH(CH3)2
These alkylations are catalyzed by various Lewis acids, such as aluminium trichloride.
m- and p-Cymene are mainly of interest as precursors to the respective cresols, which exploits the Hock rearrangements.[1]
References
- ^ a b Schmidt, Roland; Griesbaum, Karl; Behr, Arno; Biedenkapp, Dieter; Voges, Heinz-Werner; Garbe, Dorothea; Paetz, Christian; Collin, Gerd; Mayer, Dieter; Höke, Hartmut (2014). "Hydrocarbons". Ullmann's Encyclopedia of Industrial Chemistry. pp. 1–74. doi:10.1002/14356007.a13_227.pub3. ISBN 9783527306732.
- v
- t
- e
Hydrocarbons
aliphatic
hydrocarbons
| Alkanes CnH2n + 2 |
| ||||
|---|---|---|---|---|---|
| Cycloalkanes | |||||
| Alkylcycloalkanes |
| ||||
| Bicycloalkanes |
| ||||
| Polycycloalkanes |
| ||||
| Other |
|
aliphatic
hydrocarbons
| Alkenes CnH2n |
| ||||
|---|---|---|---|---|---|
| Alkynes CnH2n − 2 |
| ||||
| Cycloalkenes | |||||
| Alkylcycloalkenes |
| ||||
| Bicycloalkenes | |||||
| Cycloalkynes |
| ||||
| Dienes |
| ||||
| Other |
|
hydrocarbons
| PAHs |
| ||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Alkylbenzenes |
| ||||||||||||||||||||||
| Vinylbenzenes | |||||||||||||||||||||||
| Other |
|
 | This organic chemistry article is a stub. You can help Wikipedia by expanding it. |
- v
- t
- e
