Epoxy curing agent Knowledge Diethyl acetone-1,3-dicarboxylate Diethyl acetone-1,3-dicarboxylate

Diethyl acetone-1,3-dicarboxylate Diethyl acetone-1,3-dicarboxylate

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1,3-acetone dicarboxylic acid diethyl ester structural formula

Structural formula

Business number 02RT
Molecular formula C9H14O5
Molecular weight 202.20
label

Diethyl 3-oxoglutarate,

Diethyl 3-oxoglutarate

Numbering system

CAS number:105-50-0

MDL number:MFCD00009200

EINECS number:203-302-2

RTECS number:None

BRN number:640146

PubChem number:24850124

Physical property data

1. Properties: colorless liquid.

2. Density (g/mL, 25℃): 1.112

3. Relative vapor density (g/mL, air=1): Undetermined

4. Melting point (ºC): Undetermined

5. Boiling point (ºC, normal pressure): 250

6. Boiling point (ºC, 10mmHg): 134-135

7. Refractive index: 1.438-1.442

8. Flash point (ºC): 86

9. Specific rotation (º): Undetermined

10. Autoignition point or ignition temperature (ºC): Not determined

11. Vapor pressure (mmHg, 20ºC): Not determined

12. Saturated vapor pressure (kPa , ℃): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15 . Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) distribution coefficient: Undetermined

17. Explosion upper limit (%, V/V ): Undetermined

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: Insoluble in water, soluble in alcohol, ether and benzene.

Toxicological data

None

Ecological data

This substance is slightly hazardous to water.

Molecular structure data

1. Molar refractive index: 47.32

2. Molar volume (cm3/mol): 181.8

3. Isotonic specific volume (90.2K ): 444.7

4. Surface tension (dyne/cm): 36.3

5. Dielectric constant:

6. Dipole moment (10-24cm3):

7. Polarizability: 18.76

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 0.7

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 5

4. Number of rotatable chemical bonds: 8

5. Number of tautomers: 5

6. Topological molecule polar surface area 69.7

7. Number of heavy atoms: 14

8. Surface charge: 0

9. Complexity: 199

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Covalent bond unitQuantity:1

Properties and stability

Avoid contact with oxidants.

Storage method

Stored in a cool, ventilated warehouse. Keep away from fire and heat sources. They should be stored separately from oxidants and strong alkali, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials.

Synthesis method

1. Obtained from the reaction of 1,3-acetone dicarboxylic acid and absolute ethanol.

2. Preparation method:

Add 700mL of absolute ethanol into the reaction bottle, and pass in dry hydrogen chloride gas under cooling (can be prepared by the reaction of sodium chloride and sulfuric acid, and treated with concentrated sulfuric acid Dry) until 130-150g of hydrogen chloride is absorbed, add 460g (3.15mol) of acetone dicarboxylic acid (2) in batches while stirring. Slowly heat to 45°C until the acetone dicarboxylic acid is completely dissolved. Cool to room temperature and stir the reaction for 12 hours. Pour the reactant into 1.4L water and separate the organic layer. The aqueous layer was extracted with chloroform (500mL×2). The organic layers were combined, washed with saturated sodium bicarbonate aqueous solution, and dried over anhydrous sodium sulfate. The solvent was evaporated and then distilled under reduced pressure. The fraction at 131-136°C/1.2-1.3kPa was collected to obtain 295g of diethyl acetone dicarboxylate (1) with a yield of 46.4%. Note: ① Acetone dicarboxylic acid is unstable, so it is best not to use concentrated sulfuric acid as a catalyst for the esterification reaction. [1]

Purpose

Organic synthesis intermediates.

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