Carbazole
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Names | |
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IUPAC name
9H-carbazole
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Other names
9-azafluorene
dibenzopyrrole diphenylenimine diphenyleneimide USAF EK-600 | |
Identifiers | |
3D model (JSmol)
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3956 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
DrugBank | |
ECHA InfoCard | 100.001.542 |
EC Number |
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102490 | |
KEGG | |
PubChem CID
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RTECS number |
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C12H9N | |
Molar mass | 167.211 g·mol−1 |
Density | 1.301 g cm−3 |
Melting point | 246.3 °C (475.3 °F; 519.5 K)[1] |
Boiling point | 354.69 °C (670.44 °F; 627.84 K)[1] |
−117.4 × 10−6 cm3 mol−1 | |
Hazards | |
GHS labelling: | |
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Warning | |
H341, H351, H400, H411, H413 | |
P201, P202, P273, P281, P308+P313, P391, P405, P501 | |
Flash point | 220 °C (428 °F; 493 K) [1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Carbazole is an aromatic heterocyclic organic compound. It has a tricyclic structure, consisting of two six-membered benzene rings fused on either side of a five-membered nitrogen-containing ring. The compound's structure is based on the indole structure, but in which a second benzene ring is fused onto the five-membered ring at the 2–3 position of indole (equivalent to the 9a–4a double bond in carbazole, respectively).
Carbazole is a constituent of tobacco smoke.[2]
Synthesis
A classic laboratory organic synthesis for carbazole is the Borsche–Drechsel cyclization.[3][4]
![Borsche–Drechsel synthesis](http://upload.wikimedia.org/wikipedia/commons/thumb/2/2a/Ciclizaci%C3%B3n_de_Borsche-Drechsel2.png/300px-Ciclizaci%C3%B3n_de_Borsche-Drechsel2.png)
In the first step, phenylhydrazine is condensed with cyclohexanone to the corresponding imine. The second step is a hydrochloric acid-catalyzed rearrangement reaction and ring-closing reaction to tetrahydrocarbazole. In one modification, both steps are rolled into one by carrying out the reaction in acetic acid.[5] In the third step, this compound is oxidized by red lead to carbazole itself.
Another classic is the Bucherer carbazole synthesis, which uses a naphthol and an aryl hydrazine.[6]
![Bucherer carbazole synthesis](http://upload.wikimedia.org/wikipedia/commons/thumb/8/85/Bucherer_Carbazole_Synthesis_Scheme.png/450px-Bucherer_Carbazole_Synthesis_Scheme.png)
A third method for the synthesis of carbazole is the Graebe–Ullmann reaction.
![Graebe–Ullmann reaction](http://upload.wikimedia.org/wikipedia/commons/thumb/d/d4/Reacci%C3%B3n_de_Graebe-Ullman.png/450px-Reacci%C3%B3n_de_Graebe-Ullman.png)
In the first step, an N-phenyl-1,2-diaminobenzene (N-phenyl-o-phenylenediamine) is converted into a diazonium salt which instantaneously forms a 1,2,3-triazole. The triazole is unstable and at elevated temperatures, nitrogen is released and the carbazole is formed.[7][8]
Applications
Aminoethylcarbazole is used in the production of pigment violet 23.
![](http://upload.wikimedia.org/wikipedia/commons/thumb/3/3d/CI_Pigment_Violet_23_Synthesis.jpg/600px-CI_Pigment_Violet_23_Synthesis.jpg)
- Rimcazole is also made from carbazole proper.
- Carprofen is another use.
- NNC 05-2090 & NNC 05-2045 are both uncommon, but still technical case examples.
Related aromatic compounds
References
- ^ a b c Lide, David R. (2007). CRC Handbook of Chemistry and Physics, 88th Edition. CRC Press. pp. 3–86. ISBN 978-0-8493-0488-0.
- ^ Talhout, Reinskje; Schulz, Thomas; Florek, Ewa; Van Benthem, Jan; Wester, Piet; Opperhuizen, Antoon (2011). "Hazardous Compounds in Tobacco Smoke". Int. J. Environ. Res. Public Health. 8 (12): 613–628. doi:10.3390/ijerph8020613. PMC 3084482. PMID 21556207.
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: CS1 maint: unflagged free DOI (link) - ^ W. Borsche (1908). "Ueber Tetra- und Hexahydrocarbazolverbindungen und eine neue Carbazolsynthese. (Mitbearbeitet von. A. Witte und W. Bothe.)". Justus Liebigs Ann. Chem. (in German). 359 (1–2): 49–80. doi:10.1002/jlac.19083590103.
- ^ E. Drechsel (1888). "Ueber Elektrolyse des Phenols mit Wechselströmen". J. Prakt. Chem. (in German). 38 (1): 65–74. doi:10.1002/prac.18880380105.
- ^ Rogers, Crosby U.; Corson, B. B. (1950). "1,2,3,4-Tetrahydrocarbazole (Carbazole, 1,2,3,4-tetrahydro-)". Organic Syntheses. 30: 90. doi:10.15227/orgsyn.030.0090; Collected Volumes, vol. 4, p. 884.
- ^ Wang, Zerong (2010). "Bucherer Carbazole Synthesis". Comprehensive Organic Name Reactions and Reagents. doi:10.1002/9780470638859.conrr120.
- ^ Carl Graebe; Fritz Ullmann (1896). "Ueber eine neue Carbazolsynthese". Justus Liebigs Ann. Chem. (in German). 291 (1): 16–17. doi:10.1002/jlac.18962910104.
- ^ O. Bremer (1934). "Über die Bedeutung der Graebe-Ullmannschen Carbazolsynthese und deren Übertragung auf N-substituierte Pyridino-triazole". Justus Liebigs Ann. Chem. (in German). 514 (1): 279–291. doi:10.1002/jlac.19345140116.
External links
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