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| Section1 = {{Chembox Identifiers
| Section1 = {{Chembox Identifiers
| CASNo = 77-25-8
| CASNo = 77-25-8
| CASNo_Ref = {{Cascite|correct|CAS}}
| ChemSpiderID = 21159400
| EC_number = 201-016-2
| 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
| PubChem = 66165
| PubChem = 66165
| UNII = CEH13944YQ
| StdInChI=1S/C11H20O4/c1-5-11(6-2,9(12)14-7-3)10(13)15-8-4/h5-8H2,1-4H3
| StdInChIKey = ZKBBUZRGPULIRN-UHFFFAOYSA-N
| 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 2,2-diethylmalonate''' is a derivative of [[Diethyl malonate|Diethyl Malonate]].
'''Diethyl diethyl malonate''' or '''diethyl 2,2-diethylmalonate''' is a derivative of [[diethyl malonate|Diethyl Malonate]].
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>


== Uses ==
== Uses ==
As being a [[Diethyl malonate|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|Sodium ethoxide]].
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]].
:[[Image:Barbital Synthese.svg|390px]]
:[[Image:Barbital Synthese.svg|390px]]



Revision as of 21:23, 27 January 2024

Diethyl diethylmalonate
File:Diethyldiethylmalonate.png
Names
IUPAC name
diethyl 2,2-diethylpropanedioate
Other names
  • Diethyl diethylmalonate
  • Diethyl 2,2-diethylmalonate
.[1]
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.000.925 Edit this at Wikidata
EC Number
  • 201-016-2
UNII
  • InChI=1S/C11H20O4/c1-5-11(6-2,9(12)14-7-3)10(13)15-8-4/h5-8H2,1-4H3
    Key: ZKBBUZRGPULIRN-UHFFFAOYSA-N
  • InChI=1S/C11H20O4/c1-5-11(6-2,9(12)14-7-3)10(13)15-8-4/h5-8H2,1-4H3
  • CCC(CC)(C(=O)OCC)C(=O)OCC
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).

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

  1. ^ "Diethyl diethylmalonate". pubchem.ncbi.nlm.nih.gov.
  2. ^ "Synthesis of Barbiturates". www.erowid.org.