1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER

1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER
  • CAS No.:635-03-0
Other grades of this product :
1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER Basic information
Product Name:1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER
Synonyms:propanetetracarboxylicacidtetraethylester;1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER;TETRAETHYL PROPANE-1,1,2,3-TETRACARBOXYLATE;2,3-Bis(ethoxycarbonyl)pentanedioic acid diethyl ester;Propane-1,1,2,3-tetracarboxylic Acid Tetraethyl Ester;TetraethylPropane-1,1,2,3-tetracarboxylate>1,1,2,3-Propanetetracarboxylic acid, 1,1,2,3-tetraethyl ester
CAS:635-03-0
MF:C15H24O8
MW:332.35
EINECS:211-222-4
Product Categories:
Mol File:635-03-0.mol
1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER Chemical Properties
Boiling point 389.48°C (rough estimate)
density 1.1184
refractive index 1.4380-1.4420
form clear liquid
pka11.42±0.59(Predicted)
color Colorless to Almost colorless
InChIKeyWGEVJRBJWMGTSI-UHFFFAOYSA-N
Safety Information
MSDS Information
1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER Usage And Synthesis
Uses1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.
SynthesisCondensation of diethylfumarate and diethylmalonate to propane-1,1,2,3 tetracarboxylate. Catalyst specifications: Catalytic entity: Ph(CH2)-N+(PhmSO3-)3 · EtO- (1 milieq of EtO-), additive:: Sodium meta silicate 1 gm, Support: Charcoal 5 gm, Group IIA metal salt: Barium hydroxide, Method of preparation: Deposition precipitation. Procedure: in a 100-ml flask fitted with an efficient reflux condenser, magnetic stirrer bar and dropping funnel was charged 5 gm of catalyst. With stirring 1.6 g (0.001 mol) diethylmalonate and 25 ml dry ethanol was added. Reaction mixture was warmed and 1.4 gm (0.0081 mol) diethyl fumarate was added. Mixture was refluxed for 8 hours. Reaction mixture was cooled and suspension was centrifuged to recover catalyst. Analysis of reaction liquid indicated 90 % conversion for diethylmalonate. Product was distilled under vacuum 8 mm at 180-190°C to obtain propane-1,1,2,3 tetracarboxylate 85% yield. Catalyst was recovered and washed with ethanol, diethyl ether and dried under vacuum. Catalyst was recycled to obtain equivalent activity.
1,1,2,3-PROPANETETRACARBOXYLIC ACID TETRAETHYL ESTER Preparation Products And Raw materials

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