Chemistry:Benzil
| |
| |
| |
| Names | |
|---|---|
| Preferred IUPAC name
Diphenylethanedione | |
| Systematic IUPAC name
1,2-Diphenylethane-1,2-dione | |
| Other names
Diphenylethane-1,2-dione
Benzil Dibenzoyl Bibenzoyl Diphenylglyoxal | |
| Identifiers | |
3D model (JSmol)
|
|
| 608047 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| EC Number |
|
PubChem CID
|
|
| RTECS number |
|
| UNII | |
| |
| |
| Properties | |
| C14H10O2 | |
| Molar mass | 210.232 g·mol−1 |
| Appearance | yellow crystalline powder |
| Density | 1.23 g/cm3, solid (1.255 g/cm3, x-ray) |
| Melting point | 94.0 to 96.0 °C; 201.2 to 204.8 °F; 367.1 to 369.2 K |
| Boiling point | 346.0 to 348.0 °C; 654.8 to 658.4 °F; 619.1 to 621.1 K |
| insoluble | |
| Solubility in ethanol | soluble |
| Solubility in diethyl ether | soluble |
| Solubility in benzene | soluble |
| -118.6·10−6 cm3/mol | |
| Structure | |
| P31,221[1] | |
| 3.8 D[2] | |
| Hazards | |
| Main hazards | Irritant |
| GHS pictograms | 
|
| GHS Signal word | Warning |
| H315, H319, H335 | |
| P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
|
>3 g/kg (mouse, oral)[3] |
| Related compounds | |
Related diketones
|
diacetyl |
Related compounds
|
benzophenone glyoxal bibenzil |
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 | |
Benzil (i.e. Bz2, systematically known as 1,2-diphenylethane-1,2-dione) is the organic compound with the formula (C6H5CO)2, generally abbreviated (PhCO)2. This yellow solid is one of the most common diketones. Its main use is as a photoinitiator in polymer chemistry.[4]
Structure
The compound's most noteworthy structural feature is the long carbon-carbon bond of 1.54 Å, which indicates the absence of pi-bonding between the two carbonyl centers. The PhCO centers are planar, but the pair of benzoyl groups are twisted with respect to the other with a dihedral angle of 117°.[5] In less hindered analogues (glyoxal, biacetyl, oxalic acid derivatives), the (RCO)2 group adopts a planar, anti-conformation.
Applications
Most benzil can be used as a photoinitiator in the free-radical curing of polymer networks. It absorbs ultraviolet radiation at a wavelength of 260 nm, leading to decomposition with formation of free-radical species and formation of cross-links within the material. However, it is a relatively poor photoinitiator, and is seldom used. It undergoes photobleaching, which allows the curing light to reach deeper layers of the material on longer exposure.[6] Acetal derivatives, such as 2,2-dimethoxy-2-phenylacetophenone, have better properties for this application.[6]
Benzil is a potent inhibitor of human carboxylesterases, enzymes involved in the hydrolysis of carboxylesters and many clinically used drugs.[7]
Reactions
Benzil is a standard building block in organic synthesis. It condenses with amines to give diketimine ligands. A classic organic reaction of benzil is the benzilic acid rearrangement, in which base catalyses the conversion of benzil to benzilic acid. This reactivity is exploited in the preparation of the drug phenytoin. Benzil also reacts with 1,3-diphenylacetone in an aldol condensation to give tetraphenylcyclopentadienone.
Preparation
Benzil is prepared from benzoin, for example with copper(II) acetate:[8]
- PhC(O)CH(OH)Ph + 2 Cu2+ → PhC(O)C(O)Ph + 2 H+ + 2 Cu+
Other suitable oxidizing agents such as nitric acid (HNO3) are used routinely.
Iron(III) chloride (FeCl3) can be used as an inexpensive catalyst for this chemical conversion.[9]
References
- ↑ Acta Crystallogr. B43 398 (1987)
- ↑ Spectrochim. Acta A60 (8-9) 1805 (2004)
- ↑ "Benzil" (in en). https://pubchem.ncbi.nlm.nih.gov/compound/Benzil#section=Toxicity.
- ↑ Hardo Siegel, Manfred Eggersdorfer "Ketones" in Ullmann's Encyclopedia of Industrial Chemistry Wiley-VCH, 2002 by Wiley-VCH, Weinheim. doi:10.1002/14356007.a15_077
- ↑ Quang. Shen, Kolbjoern. Hagen "Gas-phase molecular structure and conformation of benzil as determined by electron diffraction" J. Phys. Chem., 1987, 91 (6), pp 1357–1360. doi:10.1021/j100290a017.
- ↑ 6.0 6.1 Green, W. Arthur (2010-04-22). Industrial Photoinitiators: A Technical Guide. p. 31. ISBN 9781439827468. https://books.google.com/books?id=b1jRBQAAQBAJ&dq=benzil+photoinitiator&pg=PA31. Retrieved 2022-05-21.
- ↑ Wadkins. R. M. et al "Identification and characterization of novel benzil (diphenylethane-1,2-dione) analogues as inhibitors of mammalian carboxylesterases. J. Med. Chem., 2005 48 pp 2906–15.
- ↑ Depreux, P.; Bethegnies, G.; Marcincal-Lefebvre, A. (1988). "Synthesis of benzil from benzoin with copper(II) acetate". Journal of Chemical Education 65 (6): 553. doi:10.1021/ed065p553. Bibcode: 1988JChEd..65..553D.
- ↑ Bi, Xiaoxin; Wu, Lintao; Yan, Chaoguo; Jing, Xiaobi; Zhu, Hongxiang (2011). "One-Pot Synthesis Benzils from Aldehydes Via Nhc-Catalyzed Benzoin Dimerization Under Metal-Free Conditions in Water". Journal of the Chilean Chemical Society 56 (2): 663. doi:10.4067/S0717-97072011000200008.
 |  |
