Benzonitrile

Benzonitrile
Skeletal formula	Ball-and-stick model
Names
	Preferred IUPAC name Benzonitrile
	Systematic IUPAC name Benzenecarbonitrile
	Other names cyanobenzene ; phenyl cyanide
Identifiers
CAS Number	100-47-0 ;
3D model (JSmol)	Interactive image;
3DMet	B01115;
Beilstein Reference	506893
ChEBI	CHEBI:27991 ;
ChEMBL	ChEMBL15819 ;
ChemSpider	7224 ;
ECHA InfoCard	100.002.596
EC Number	202-855-7;
Gmelin Reference	2653
KEGG	C09814 ;
PubChem CID	7505;
RTECS number	DI2450000;
UNII	9V9APP5H5S ;
UN number	2224
CompTox Dashboard (EPA)	DTXSID7021491 ;
	InChI InChI=1S/C7H5N/c8-6-7-4-2-1-3-5-7/h1-5H Key: JFDZBHWFFUWGJE-UHFFFAOYSA-N ; InChI=1/C7H5N/c8-6-7-4-2-1-3-5-7/h1-5H Key: JFDZBHWFFUWGJE-UHFFFAOYAY;
	SMILES N#Cc1ccccc1;
Properties
Chemical formula	C6H5(CN)
Molar mass	103.12 g/mol
Density	1.0 g/ml
Melting point	−13 °C (9 °F; 260 K)
Boiling point	188 to 191 °C (370 to 376 °F; 461 to 464 K)
Solubility in water	<0.5 g/100 ml (22 °C)
Magnetic susceptibility (χ)	-65.19·10−6 cm3/mol
Refractive index (nD)	1.5280
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H302, H312
Precautionary statements	P264, P270, P280, P301+P312, P302+P352, P312, P322, P330, P363, P501
NFPA 704 (fire diamond)	3 2 0
Flash point	75 °C (167 °F; 348 K)
Autoignition; temperature	550 °C (1,022 °F; 823 K)
Explosive limits	1.4–7.2%
	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

Benzonitrile is the chemical compound with the formula C₆H₅(CN), abbreviated PhCN. This aromatic organic compound is a colorless liquid with a sweet bitter almond odour. It is mainly used as a precursor to the resin benzoguanamine.

Production

It is prepared by ammoxidation of toluene, that is its reaction with ammonia and oxygen (or air) at 400 to 450 °C (752 to 842 °F).^[1]

C₆H₅CH₃ + 3/2 O₂ + NH₃ → C₆H₅(CN) + 3 H₂O

In the laboratory it can be prepared by the dehydration of benzamide or benzaldehyde oxime^[2] or by the Rosenmund–von Braun reaction using cuprous cyanide or NaCN/DMSO and bromobenzene.

Applications

Laboratory uses

Benzonitrile is a useful solvent and a versatile precursor to many derivatives. It reacts with amines to afford N-substituted benzamides after hydrolysis.^[3] It is a precursor to diphenylmethanimine via reaction with phenylmagnesium bromide followed by methanolysis.^[4]

Benzonitrile forms coordination complexes with transition metals that are both soluble in organic solvents and conveniently labile. One example is PdCl₂(PhCN)₂. The benzonitrile ligands are readily displaced by stronger ligands, making benzonitrile complexes useful synthetic intermediates.^[5]

History

Benzonitrile was reported by Hermann Fehling in 1844. He found the compound as a product from the thermal dehydration of ammonium benzoate. He deduced its structure from the already known analogue reaction of ammonium formate yielding hydrogen cyanide (formonitrile). He also coined the name benzonitrile which gave the name to all the group of nitriles.^[6]

In 2018, benzonitrile was reported to be detected in the interstellar medium.^[7]

References

^ Maki, Takao; Takeda, Kazuo (June 2000). "Benzoic Acid and Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a03_555. ISBN 3527306730.
^ Loupy, André; Régnier, Serge (August 1999). "Solvent-free microwave-assisted Beckmann rearrangement of benzaldehyde and 2-hydroxyacetophenone oximes". Tetrahedron Letters. 40 (34): 6221–6224. doi:10.1016/S0040-4039(99)01159-4. ISSN 0040-4039.
^ Cooper, F. C.; Partridge, M. W. (1963). "N-Phenylbenzamidine". Organic Syntheses; Collected Volumes, vol. 4, p. 769.
^ Pickard, P. L.; Tolbert, T. L. (1973). "Diphenyl Ketimine". Organic Syntheses; Collected Volumes, vol. 5, p. 520.
^ Anderson, Gordon K.; Lin, Minren (1990). "Bis(Benzonitrile)Dichloro Complexes of Palladium and Platinum". Reagents for Transition Metal Complex and Organometallic Syntheses. Inorganic Syntheses. Vol. 28. John Wiley & Sons. pp. 60–63. doi:10.1002/9780470132593.ch13. ISBN 978-0-470-13259-3.
^ Fehling, Hermann (1844). "Ueber die Zersetzung des benzoësauren Ammoniaks durch die Wärme". Annalen der Chemie und Pharmacie. 49 (1): 91–97. doi:10.1002/jlac.18440490106.
^ McGuire, Brett A.; et al. (January 2018). "Detection of the aromatic molecule benzonitrile (c\sC6H5CN) in the interstellar medium". Science. 359 (6372): 202–205. arXiv:1801.04228. Bibcode:2018Sci...359..202M. doi:10.1126/science.aao4890. PMID 29326270. S2CID 206663501.

External links

International Chemical Safety Card 1103

[1] Maki, Takao; Takeda, Kazuo (June 2000). "Benzoic Acid and Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a03_555. ISBN 3527306730.

[2] Loupy, André; Régnier, Serge (August 1999). "Solvent-free microwave-assisted Beckmann rearrangement of benzaldehyde and 2-hydroxyacetophenone oximes". Tetrahedron Letters. 40 (34): 6221–6224. doi:10.1016/S0040-4039(99)01159-4. ISSN 0040-4039.

[3] Cooper, F. C.; Partridge, M. W. (1963). "N-Phenylbenzamidine". Organic Syntheses; Collected Volumes, vol. 4, p. 769.

[4] Pickard, P. L.; Tolbert, T. L. (1973). "Diphenyl Ketimine". Organic Syntheses; Collected Volumes, vol. 5, p. 520.

[5] Anderson, Gordon K.; Lin, Minren (1990). "Bis(Benzonitrile)Dichloro Complexes of Palladium and Platinum". Reagents for Transition Metal Complex and Organometallic Syntheses. Inorganic Syntheses. Vol. 28. John Wiley & Sons. pp. 60–63. doi:10.1002/9780470132593.ch13. ISBN 978-0-470-13259-3.

[6] Fehling, Hermann (1844). "Ueber die Zersetzung des benzoësauren Ammoniaks durch die Wärme". Annalen der Chemie und Pharmacie. 49 (1): 91–97. doi:10.1002/jlac.18440490106.

[SC-20180112-7] McGuire, Brett A.; et al. (January 2018). "Detection of the aromatic molecule benzonitrile (c\sC6H5CN) in the interstellar medium". Science. 359 (6372): 202–205. arXiv:1801.04228. Bibcode:2018Sci...359..202M. doi:10.1126/science.aao4890. PMID 29326270. S2CID 206663501.

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