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{{Short description|Intermediate Chemical in H2O2 Synthesis}}
{{chembox
{{Chembox
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| verifiedrevid = 413109678
| Verifiedfields = changed
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| verifiedrevid = 477213314
| Name = 2-Ethylanthraquinone
| Name = 2-Ethylanthraquinone
| ImageFile = 2-Ethylanthraquinone.svg
| ImageFile = 2-Ethylanthraquinone.svg
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| ImageName1 = Ball-and-stick model
| ImageName1 = Ball-and-stick model
| ImageSize1 = 230px
| ImageSize1 = 230px
| PIN = 2-Ethylanthracene-9,10-dione
| OtherNames = 2-Ethyl-9,10-anthracenedione
| OtherNames = 2-Ethyl-9,10-anthracenedione
| Section1 = {{Chembox Identifiers
| Section1 = {{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 6514
| ChemSpiderID = 6514
| PubChem = 6772
| UNII = 59YJ81QZKD
| InChI = 1/C16H12O2/c1-2-10-7-8-13-14(9-10)16(18)12-6-4-3-5-11(12)15(13)17/h3-9H,2H2,1H3
| InChI = 1/C16H12O2/c1-2-10-7-8-13-14(9-10)16(18)12-6-4-3-5-11(12)15(13)17/h3-9H,2H2,1H3
| InChIKey = SJEBAWHUJDUKQK-UHFFFAOYAW
| InChIKey = SJEBAWHUJDUKQK-UHFFFAOYAW
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = SJEBAWHUJDUKQK-UHFFFAOYSA-N
| StdInChIKey = SJEBAWHUJDUKQK-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|changed|??}}
| CASNo = 84-51-5
| CASNo = 84-51-5
| EINECS = 201-535-4
| EINECS = 201-535-4
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}}
}}
| Section7 = {{Chembox Hazards
| Section7 = {{Chembox Hazards
⚫
| FlashPtC = 155.4
| SPhrases = {{S24}} {{S25}}
| GHSPictograms = {{GHS08}}{{GHS09}}
⚫
| FlashPt = 155.4°C,
| GHSSignalWord = Danger
| HPhrases = {{H-phrases|350|373|410}}
| PPhrases = {{P-phrases|201|202|260|273|281|308+313|314|391|405|501}}
}}
}}
}}
}}


'''2-Ethylanthraquinone''' is an [[organic compound]] that is a derivative of [[anthraquinone]]. This pale yellow solid is used in the industrial production of [[hydrogen peroxide]] (H<sub>2</sub>O<sub>2</sub>).<ref>{{cite encyclopedia |author1=Goor, G. |author2=Glenneberg, J. |author3=Jacobi, S. | title = Hydrogen Peroxide | encyclopedia = Ullmann's Encyclopedia of Industrial Chemistry | year = 2007 | publisher = Wiley-VCH | location = Weinheim | doi = 10.1002/14356007.a13_443.pub2 |isbn=9783527303854 }}</ref><ref>Römpp CD 2006, Georg Thieme Verlag 2006</ref>
'''2-Ethylanthraquinone''' also called'''2-Ethyl-9,10-anthraquinone''' ‎ is an [[aromatic]] [[organic compound]] closely related to [[anthracene]].


==Production==
It is commonly used to make [[2-ethyl-9,10-dihydroxyanthracene]] and to create [[hydrogen peroxide]] (H<sub>2</sub>O<sub>2</sub>)with the regeneration of 2-Ethylanthraquinone by the Riedl-Pfleiderer, or [[autoxidation]], process:
2-Ethylanthraquinone is prepared from the reaction of [[phthalic anhydride]] and [[ethylbenzene]]:
:C<sub>6</sub>H<sub>4</sub>(CO)<sub>2</sub>O + C<sub>6</sub>H<sub>5</sub>Et → C<sub>6</sub>H<sub>4</sub>(CO)<sub>2</sub>C<sub>6</sub>H<sub>3</sub>Et + H<sub>2</sub>O.
Both phthalic anhydride and ethylbenzene are readily available, being otherwise used in the large-scale production of plastics.


==Uses==
⚫
[[Image:Riedl-Pfleiderer process.svg|left|400px|The Riedl-Pfleiderer process.]]<br style="clear:left;"/>
[[Hydrogen peroxide]] is produced industrially by the [[anthraquinone process]] which involves using 2-alkyl-9,10-anthraquinones for hydrogenation. Many derivatives of anthraquinone are used but 2-ethylanthraquinone is common because of its high selectivity. The hydrogenation of the unsubstituted ring can reach 90% selectivity by using 2-ethylanthraquinone. Hydrogenation follows the Riedl-Pfleiderer, or [[autoxidation]], process:


⚫
[[File:Riedl-Pfleiderer process.svg|left|400px|The Riedl-Pfleiderer process.]]{{clear|left}}
⚫
{{DEFAULTSORT:Ethylanthraquinone, 2-}}
The [[hydrogenation]] of [[2-ethylanthraquinone]] is catalyzed by [[palladium]]. Hydrogenation produces both 2-ethylanthrahydroquinone and tetrahydroanthraquinone. The tetrahydro derivative of 2-alkylanthraquinone is easily hydrogenated but is more difficult to oxidize. The formation of the tetrahydro derivative can be suppressed through the selection of catalysts, solvents, and reaction conditions. Some suggested solvent mixtures are polyalkylated benzenes and alkyl phosphates or tetraalkyl ureas, trimethylbenzenes and alkylcyclohexanol esters, and methylnaphthalene and nonyl alcohols.


==References==
<references />


⚫
{{DEFAULTSORT:Ethylanthraquinone, 2-}}
{{aromatic-stub}}

[[Category:Anthraquinones]]
[[Category:Anthraquinones]]

Latest revision as of 10:04, 13 January 2024

2-Ethylanthraquinone
Structural formula of 2-Ethylanthraquinone
Ball-and-stick model
Names
Preferred IUPAC name
2-Ethylanthracene-9,10-dione
Other names
2-Ethyl-9,10-anthracenedione
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.001.396 Edit this at Wikidata
EC Number
  • 201-535-4
UNII
  • InChI=1S/C16H12O2/c1-2-10-7-8-13-14(9-10)16(18)12-6-4-3-5-11(12)15(13)17/h3-9H,2H2,1H3 checkY
    Key: SJEBAWHUJDUKQK-UHFFFAOYSA-N checkY
  • InChI=1/C16H12O2/c1-2-10-7-8-13-14(9-10)16(18)12-6-4-3-5-11(12)15(13)17/h3-9H,2H2,1H3
    Key: SJEBAWHUJDUKQK-UHFFFAOYAW
  • O=C2c1c(cccc1)C(=O)c3c2ccc(c3)CC
Properties
C16H12O2
Molar mass 236.27 g/mol
Appearance white to yellowish crystals or powder
Density 1.231g/cm3
Melting point 105 °C (221 °F; 378 K)
Boiling point 415.4 @ 760mmHg
Hazards
GHS labelling:
GHS08: Health hazardGHS09: Environmental hazard
Danger
H350, H373, H410
P201, P202, P260, P273, P281, P308+P313, P314, P391, P405, P501
Flash point 155.4 °C (311.7 °F; 428.5 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

2-Ethylanthraquinone is an organic compound that is a derivative of anthraquinone. This pale yellow solid is used in the industrial production of hydrogen peroxide (H2O2).[1][2]

Production

[edit]

2-Ethylanthraquinone is prepared from the reaction of phthalic anhydride and ethylbenzene:

C6H4(CO)2O + C6H5Et → C6H4(CO)2C6H3Et + H2O.

Both phthalic anhydride and ethylbenzene are readily available, being otherwise used in the large-scale production of plastics.

Uses

[edit]

Hydrogen peroxide is produced industrially by the anthraquinone process which involves using 2-alkyl-9,10-anthraquinones for hydrogenation. Many derivatives of anthraquinone are used but 2-ethylanthraquinone is common because of its high selectivity. The hydrogenation of the unsubstituted ring can reach 90% selectivity by using 2-ethylanthraquinone. Hydrogenation follows the Riedl-Pfleiderer, or autoxidation, process:

The Riedl-Pfleiderer process.
The Riedl-Pfleiderer process.

The hydrogenation of 2-ethylanthraquinone is catalyzed by palladium. Hydrogenation produces both 2-ethylanthrahydroquinone and tetrahydroanthraquinone. The tetrahydro derivative of 2-alkylanthraquinone is easily hydrogenated but is more difficult to oxidize. The formation of the tetrahydro derivative can be suppressed through the selection of catalysts, solvents, and reaction conditions. Some suggested solvent mixtures are polyalkylated benzenes and alkyl phosphates or tetraalkyl ureas, trimethylbenzenes and alkylcyclohexanol esters, and methylnaphthalene and nonyl alcohols.

References

[edit]
  1. ^ Goor, G.; Glenneberg, J.; Jacobi, S. (2007). "Hydrogen Peroxide". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a13_443.pub2. ISBN 9783527303854.
  2. ^ Römpp CD 2006, Georg Thieme Verlag 2006
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