Diethyl diethylmalonate: Difference between revisions
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| Section1 = {{Chembox Identifiers |
| Section1 = {{Chembox Identifiers |
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| CASNo = 77-25-8 |
| CASNo = 77-25-8 |
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| CASNo_Ref = {{Cascite|correct|CAS}} |
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| ChemSpiderID = 21159400 |
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| EC_number = 201-016-2 |
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| InChI = 1S/C11H20O4/c1-5-11(6-2,9(12)14-7-3)10(13)15-8-4/h5-8H2,1-4H3 |
| InChI = 1S/C11H20O4/c1-5-11(6-2,9(12)14-7-3)10(13)15-8-4/h5-8H2,1-4H3 |
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| PubChem = 66165 |
| PubChem = 66165 |
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| UNII = CEH13944YQ |
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| StdInChI=1S/C11H20O4/c1-5-11(6-2,9(12)14-7-3)10(13)15-8-4/h5-8H2,1-4H3 |
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| StdInChIKey = ZKBBUZRGPULIRN-UHFFFAOYSA-N |
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| SMILES = CCC(CC)(C(=O)OCC)C(=O)OCC |
| SMILES = CCC(CC)(C(=O)OCC)C(=O)OCC |
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'''Diethyl diethyl malonate''' or ''' |
'''Diethyl diethyl malonate''' or '''diethyl 2,2-diethylmalonate''' is a derivative of [[diethyl malonate|Diethyl Malonate]]. |
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It can be used in the synthesis of [[Barbital]]<ref>{{Cite web|url=https://www.erowid.org/archive/rhodium/chemistry/barbiturates.html|title=Synthesis of Barbiturates|website=www.erowid.org}}</ref> |
It can be used in the synthesis of [[Barbital]]<ref>{{Cite web|url=https://www.erowid.org/archive/rhodium/chemistry/barbiturates.html|title=Synthesis of Barbiturates|website=www.erowid.org}}</ref> |
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== Uses == |
== Uses == |
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As being a [[ |
As being a [[diethyl malonate]] derivative, it can be combined with [[Urea]] under the action of a strong base to form a [[Barbiturate]]. In this case, diethyl diethyl malonate + [[urea]] forms [[barbital]] under the action of [[sodium ethoxide]]. |
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:[[Image:Barbital Synthese.svg|390px]] |
:[[Image:Barbital Synthese.svg|390px]] |
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Revision as of 21:23, 27 January 2024
File:Diethyldiethylmalonate.png | |
Names | |
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IUPAC name
diethyl 2,2-diethylpropanedioate
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Other names
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.000.925 |
EC Number |
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PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C11H20O4 | |
Molar mass | 216.27 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Diethyl diethyl malonate or diethyl 2,2-diethylmalonate is a derivative of Diethyl Malonate. It can be used in the synthesis of Barbital[2]
Uses
As being a diethyl malonate derivative, it can be combined with Urea under the action of a strong base to form a Barbiturate. In this case, diethyl diethyl malonate + urea forms barbital under the action of sodium ethoxide.
References
- ^ "Diethyl diethylmalonate". pubchem.ncbi.nlm.nih.gov.
- ^ "Synthesis of Barbiturates". www.erowid.org.