2-Nitrobenzaldehyde (original) (raw)
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Names | |
Preferred IUPAC name 2-Nitrobenzaldehyde | |
Other namesNitrobenzaldehyde_ortho_-Nitrobenzaldehyde_o_-Nitrobenzaldehyde | |
Identifiers | |
CAS Number | 552-89-6 Y |
3D model (JSmol) | Interactive image |
ChEBI | CHEBI:66927 |
ChEMBL | ChEMBL166559 Y |
ChemSpider | 10630 Y |
ECHA InfoCard | 100.008.206 |
EC Number | 209-025-3 |
PubChem CID | 11101 |
UNII | 48B18Q9B8E Y |
CompTox Dashboard (EPA) | DTXSID0022060 |
InChI InChI=1S/C7H5NO3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-5H YKey: CMWKITSNTDAEDT-UHFFFAOYSA-N YInChI=1/C7H5NO3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-5HKey: CMWKITSNTDAEDT-UHFFFAOYAD | |
SMILES O=[N+]([O-])c1ccccc1C=O | |
Properties | |
Chemical formula | C7H5NO3 |
Molar mass | 151.12 g/mol |
Appearance | Pale yellow crystalline powder |
Melting point | 43 °C (109 °F; 316 K) |
Boiling point | 152 °C (306 °F; 425 K) |
Solubility in water | Insoluble |
Magnetic susceptibility (χ) | -68.23·10−6 cm3/mol |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards | Harmful, Potentially mutagenic |
GHS labelling:[3] | |
Pictograms | |
Signal word | Warning |
Hazard statements | H302, H315, H319, H335, H412 |
Precautionary statements | P261, P264, P270, P271, P273, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501 |
NFPA 704 (fire diamond) | 2 1 0 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references |
Chemical compound
2-Nitrobenzaldehyde is an organic compound with the formula O2NC6H4CHO. It is one of three isomers of nitrobenzaldehyde. It contains a nitro group adjacent to the formyl group.[4]
The main routes to nitrobenzaldehyde begin with the nitration of styrene or cinnamic acid followed by the conversions of the resulting 2-nitrostyrene and 2-nitrocinnamic acids, respectively. Cinnamaldehyde can also be nitrated, e.g., in a solution of acetic anhydride in acetic acid, in high-yield to 2-nitrocinnamaldehyde.[5] This compound is then oxidized to 2-nitrocinnamic acid, which is decarboxylated to the 2-nitrostyrene. The vinyl group can be oxidized in a number of different ways to yield 2-nitrobenzaldehyde.[6]
In one synthetic process, toluene is mono-nitrated at cold temperatures to 2-nitrotoluene, with about 58% being converted to the ortho- isomer, the remaining forming meta- and para- isomers.[7] The 2-nitrotoluene can then be oxidized to yield 2-nitrobenzaldehyde.[8][9]
Alternatively, 2-nitrotoluene as formed above can be halogenated to a 2-nitrobenzyl halide followed by oxidation with DMSO and sodium bicarbonate to yield 2-nitrobenzaldehyde, which is subsequently purified with the creation of a bisulfite adduct.[10]
The nitration of benzaldehyde produces mostly 3-nitrobenzaldehyde, with yields being about 19% for the ortho-, 72% for the meta- and 9% for the para isomer.[11] For this reason, the nitration of benzaldehyde to yield 2-nitrobenzaldehyde is not cost-effective.
2-Nitrobenzaldehyde is an intermediate in an early route to indigo, a water-insoluble dye commonly used to dye jeans and other fabrics. In the Baeyer-Drewson indigo synthesis, 2-nitrobenzaldehyde condenses with acetone in basic aqueous solution to yield indigo in a one-pot synthesis.[12][13][14][15] The method was abandoned in the early part of the 20th century, being replaced by routes from aniline.[16]
Baeyer-Drewson Indigo Synthesis
Given its two relatively reactive groups, 2-nitrobenzaldehyde is a potential starting material for other compounds. Substituted 2-nitrobenzaldehydes can also be used to yield other important compounds based on indigo, such as indigo carmine.
2-Nitrobenzaldehyde has been shown to be a useful photoremovable protecting group for various functions.[17][18]
- ^ 2-Nitrobenzaldehyde
- ^ "2-Nitrobenzaldehyde MSDS". Archived from the original on 2011-07-07. Retrieved 2009-07-18.
- ^ "2-Nitrobenzaldehyde". pubchem.ncbi.nlm.nih.gov.
- ^ Brühne, Friedrich; Wright, Elaine (2011). "Benzaldehyde". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a03_463.pub2. ISBN 978-3-527-30385-4.
- ^ o-NITROCINNAMALDEHYDE, nitration of cinnamaldehyde, organic-synthesis
- ^ Feng, Bo; Hou, Zhenshan; Wang, Xiangrui; Hu, Yu; Li, Huan; Qiao, Yunxiang (2009-09-01). "Selective aerobic oxidation of styrene to benzaldehyde catalyzed by water-soluble palladium(II) complex in water". Green Chemistry. 11 (9): 1446–1452. doi:10.1039/B900807A. ISSN 1463-9270.
- ^ http://www.thecatalyst.org/experiments/AndersonS/AndersonS.html Product Distribution in the Nitration of Toluene, Steven W. Anderson, January 7, 1999
- ^ Synthesis of 2-Nitrobenzaldehyde from 2-Nitrotoluene Archived 2011-06-05 at the Wayback Machine, Alexander Popkov
- ^ "o-Nitrobenzaldehyde". Archived from the original on 2011-06-06. Retrieved 2009-07-21.
- ^ "Process for the Preparation of 2-Nitrobenzaldehyde". Retrieved 2010-10-18.
- ^ Structure of Benzene, California State University Dominguez Hills
- ^ See Baeyer-Drewson indigo synthesis
- ^ Synthesis of Indigo Archived 2010-06-20 at the Wayback Machine
- ^ "Indigo Synthesis". Archived from the original on 2011-07-20. Retrieved 2009-07-18.
- ^ "Synthesis of Indigo and Vat Dyeing" (PDF). Archived from the original (PDF) on 2011-07-20. Retrieved 2009-07-18.
- ^ Wiley-VCH, ed. (2003-03-11). Ullmann's Encyclopedia of Industrial Chemistry (1 ed.). Wiley. doi:10.1002/14356007.a14_149.pub2. ISBN 978-3-527-30385-4.
- ^ Šebej, Peter; Šolomek, Tomáš; Hroudná, Ľubica; Brancová, Pavla; Klán, Petr (2009). "Photochemistry of 2-Nitrobenzylidene Acetals". J. Org. Chem. 74 (22): 8647–8658. doi:10.1021/jo901756r. PMID 19824651.
- ^ Kristine L. Willett; Ronald A. Hites (2000). "Chemical Actinometry: Using o-Nitrobenzaldehyde to Measure Lamp Intensity in Photochemical Experiments". J. Chem. Educ. 77 (7): 900. Bibcode:2000JChEd..77..900W. doi:10.1021/ed077p900.