1,8-Diaminonaphthalene: Difference between revisions
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| ImageFile=Chemical structural formula of 1,8-diaminonaphthalene.svg |
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| PIN=Naphthalene-1,8-diamine |
| PIN=Naphthalene-1,8-diamine |
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| OtherNames= Deltamin, 1,8-Naphthalenediamine |
| OtherNames= Deltamin, 1,8-Naphthalenediamine |
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It is prepared by reduction of 1,8-dinitronaphthalene, which in turn is obtained as a mixture of isomers by nitration of 1-nitronaphthalene. |
It is prepared by reduction of 1,8-dinitronaphthalene, which in turn is obtained as a mixture of isomers by nitration of 1-nitronaphthalene. |
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Upon treatment with [[phthalic anhydride]] derivatives, the diamine converts to phthaloperinones.<ref>{{cite journal |doi=10.1021/ol201973w|title=Green Synthesis of Polycyclic Benzimidazole Derivatives and Organic Semiconductors|year=2011|last1=Mamada|first1=Masashi|last2=PéRez-BolíVar|first2=César|last3=Anzenbacher|first3=Pavel|journal=Organic Letters|volume=13|issue=18|pages=4882–4885|pmid=21863817|url=https://scholarworks.bgsu.edu/chem_pub/145}}</ref> The derivative from phthalic anhydride itself, Solvent Orange 60, is a useful orange pigment. It is a precursor to [[1,8-bis(dimethylamino)naphthalene]]. This compound used to produce perimidines by various aldehydes.<ref>{{ |
Upon treatment with [[phthalic anhydride]] derivatives, the diamine converts to phthaloperinones.<ref>{{cite journal |doi=10.1021/ol201973w|title=Green Synthesis of Polycyclic Benzimidazole Derivatives and Organic Semiconductors|year=2011|last1=Mamada|first1=Masashi|last2=PéRez-BolíVar|first2=César|last3=Anzenbacher|first3=Pavel|journal=Organic Letters|volume=13|issue=18|pages=4882–4885|pmid=21863817|s2cid=32185653 |url=https://scholarworks.bgsu.edu/chem_pub/145}}</ref> The derivative from phthalic anhydride itself, Solvent Orange 60, is a useful orange pigment. It is a precursor to [[1,8-bis(dimethylamino)naphthalene]]. This compound used to produce perimidines by various aldehydes.<ref>{{cite journal|last=F.K. Behbahani, F.M.Golchin|doi=10.1016/j.jtusci.2015.10.004|title=A new catalyst for the synthesis of 2-substituted perimidines catalysed by FePO4|journal=Journal of Taibah University for Science|year=2017|volume=11|issue=1 |pages=85–89|s2cid=98648448|doi-access=free|bibcode=2017JTUS...11...85B |url=https://zenodo.org/records/3593823/files/A%20new%20catalyst%20for%20the%20synthesis%20of%202%20substituted%20perimidines%20catalysed%20by%20FePO4(1).pdf}}</ref> |
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==See also== |
==See also== |
Latest revision as of 20:51, 22 February 2024
Names | |
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Preferred IUPAC name
Naphthalene-1,8-diamine | |
Other names
Deltamin, 1,8-Naphthalenediamine
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Identifiers | |
3D model (JSmol)
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ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.006.846 |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C10H10N2 | |
Molar mass | 158.1998 |
Related compounds | |
Related Aromatic amines
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1-Naphthylamine 1,8-bis(dimethylamino)naphthalene |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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1,8-Diaminonaphthalene is an organic compound with the formula C10H6(NH2)2. It is one of several isomeric naphthalenediamines. It is a colorless solid that darkens in air due to oxidation. It is a precursor to commercial pigments.[1]
Synthesis and reactions[edit]
It is prepared by reduction of 1,8-dinitronaphthalene, which in turn is obtained as a mixture of isomers by nitration of 1-nitronaphthalene.
Upon treatment with phthalic anhydride derivatives, the diamine converts to phthaloperinones.[2] The derivative from phthalic anhydride itself, Solvent Orange 60, is a useful orange pigment. It is a precursor to 1,8-bis(dimethylamino)naphthalene. This compound used to produce perimidines by various aldehydes.[3]
See also[edit]
References[edit]
- ^ Booth, Gerald (2005). "Naphthalene Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. ISBN 978-3527306732..
- ^ Mamada, Masashi; PéRez-BolíVar, César; Anzenbacher, Pavel (2011). "Green Synthesis of Polycyclic Benzimidazole Derivatives and Organic Semiconductors". Organic Letters. 13 (18): 4882–4885. doi:10.1021/ol201973w. PMID 21863817. S2CID 32185653.
- ^ F.K. Behbahani, F.M.Golchin (2017). "A new catalyst for the synthesis of 2-substituted perimidines catalysed by FePO4" (PDF). Journal of Taibah University for Science. 11 (1): 85–89. Bibcode:2017JTUS...11...85B. doi:10.1016/j.jtusci.2015.10.004. S2CID 98648448.