Cyclohexylbenzene

Cyclohexylbenzene is the organic compound with the formula C6H5-C6H11. It is a derivative of benzene with a cyclohexyl substituent (C6H11). A colorless liquid, it is produced by the alkylation of benzene with cyclohexene.[1] It is generated by the hydrodesulfurization of dibenzothiophene.[2]

Cyclohexylbenzene
Names
Preferred IUPAC name
Cyclohexylbenzene
Other names
Phenylcyclohexane
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.011.429
EC Number
  • 212-572-0
Properties
C12H16
Molar mass 160.260 g·mol−1
Appearance colorless liquid
Density 0.982 g/cm3
Melting point 7.3 °C (45.1 °F; 280.4 K)
Boiling point 240.1 °C (464.2 °F; 513.2 K)
Hazards
GHS pictograms
GHS Signal word Danger
GHS hazard statements
H302, H304, H315, H319, H400, H410
P264, P270, P273, P280, P301+310, P301+312, P302+352, P305+351+338, P321, P330, P331, P332+313, P337+313, P362, P391, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

A route to phenol analogous to the cumene process begins with cyclohexylbenzene, which is oxidized to a hydroperoxide, akin to the production of cumene hydroperoxide. Via the Hock rearrangement, cyclohexylbenzene hydroperoxide cleaves to give phenol and cyclohexanone. Cyclohexanone is an important precursor to some nylons.[3]

References

  1. Qiao, Kun; Yokoyama, Chiaki (2004). "Novel Acidic Ionic Liquids Catalytic Systems for Friedel–Crafts Alkylation of Aromatic Compounds with Alkenes". Chemistry Letters. 33 (4): 472–473. doi:10.1246/cl.2004.472.
  2. Bai, Jin; Li, Xiang; Wang, Anjie; Prins, Roel; Wang, Yao (2012). "Hydrodesulfurization of Dibenzothiophene and its Hydrogenated Intermediates over Bulk MoP". Journal of Catalysis. 287: 161–169. doi:10.1016/j.jcat.2011.12.018.
  3. Plotkin, Jeffrey S. (2016-03-21). "What's New in Phenol Production?". American Chemical Society. Archived from the original on 2019-10-27. Retrieved 2018-01-02.
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