Chemistry:Benzoic anhydride
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Names | |
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Preferred IUPAC name
Benzoic anhydride | |
Other names
Benzoic acid anhydride
Benzoyl anhydride Benzoyl benzoate | |
Identifiers | |
3D model (JSmol)
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516726 | |
ChemSpider | |
EC Number |
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PubChem CID
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UNII | |
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Properties | |
C14H10O3 | |
Molar mass | 226.23 g mol−1 |
Appearance | White to off-white solid |
Density | 1.1989 g cm−3 at 15 °C |
Melting point | 42 °C (108 °F; 315 K) |
Boiling point | 360 °C (680 °F; 633 K) |
-124.9·10−6 cm3/mol | |
Hazards | |
NFPA 704 (fire diamond) | |
Flash point | 113[2] °C (235 °F; 386 K) |
Related compounds | |
Related compounds
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Benzoic acid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Benzoic anhydride is the organic compound with the formula (C6H5CO)2O. It is the acid anhydride of benzoic acid and the simplest symmetrical aromatic acid anhydride. It is a white solid.
Preparation and reactions
It is usually prepared by the dehydration reaction of benzoic acid, e.g. using acetic anhydride:[3]
- 2 C6H5CO2H + (CH3CO)2O → (C6H5CO)2O + 2 CH3CO2H
Alternatively, sodium benzoate can be treated with benzoyl chloride. It can be produced by dehydrating benzoic acid by heating. [citation needed]
Benzoic anhydride provides a convenient way to prepare benzoic esters:
- (C6H5CO)2O + ROH → C6H5CO2H + C6H5CO2R
References
- ↑ "Sciencelab msds". http://www.sciencelab.com/msds.php?msdsId=9923052.
- ↑ "aldrich product page". http://www.sigmaaldrich.com/catalog/product/aldrich/385980?lang=hu®ion=HU.
- ↑ H. T. Clarke; E. J. Rahrs (1923). "Benzoic Anhydride". Org. Synth. 3: 21. doi:10.15227/orgsyn.003.0021.
Original source: https://en.wikipedia.org/wiki/Benzoic anhydride.
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