Basic information Safety Supplier Related

2,5-FURANDICARBOXYLIC ACID DIETHYL ESTER

Basic information Safety Supplier Related

2,5-FURANDICARBOXYLIC ACID DIETHYL ESTER Basic information

Product Name:
2,5-FURANDICARBOXYLIC ACID DIETHYL ESTER
Synonyms:
  • Diethyl furan-2,5-dicarboxylate 99%
  • Diethyl furan-2,5-dicarboxylate
  • 2,5-FURANDICARBOXYLIC ACID DIETHYL ESTER
  • Furan-2,5-dicarboxylic Acid Diethyl Ester
  • 2,5-Furandicarboxylic acid, 2,5-diethyl ester
  • Diethyl 2,5-furandicarboxylate
  • 2,5-Furandicarboxylic diethyl ester
CAS:
53662-83-2
MF:
C10H12O5
MW:
212.2
Product Categories:
  • Heterocyclic Compounds
  • Heterocycles
Mol File:
53662-83-2.mol
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2,5-FURANDICARBOXYLIC ACID DIETHYL ESTER Chemical Properties

Melting point:
46-48°C
Boiling point:
167-1680C/15Torr
Density 
1.172±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Solid
color 
White
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Safety Information

HS Code 
2932190090
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2,5-FURANDICARBOXYLIC ACID DIETHYL ESTER Usage And Synthesis

Chemical Properties

White Solid

Uses

2,5-Furandicarboxylic Acid Diethyl Ester (cas# 53662-83-2) is a compound useful in organic synthesis.

Synthesis

3238-40-2

64-17-5

53662-83-2

To a solution of 2,5-furandicarboxylic acid (1.00 g, 6.41 mmol) in anhydrous ethanol (50 mL) was slowly added 98% aqueous sulfuric acid (0.05 mL), and the reaction mixture was heated and refluxed under nitrogen protection for 18 hours. Upon completion of the reaction, the solution was cooled to room temperature and subsequently concentrated under reduced pressure to remove the solvent. The concentrated residue was separated by filtration and washed sequentially with saturated aqueous sodium bicarbonate solution (3 x 10 mL) and deionized water (3 x 10 mL) to afford finally diethyl furan-2,5-dicarboxylate as a white solid (1.33 g, 98% yield). The structure of the product was confirmed by nuclear magnetic resonance hydrogen spectroscopy (1H NMR, 500 MHz, CDCl3) and carbon spectroscopy (13C NMR, 125 MHz, CDCl3) with the following data: 1H NMR δ 1.38 (t, J = 7.1 Hz, 6H), 4.39 (q, J = 7.1 Hz, 4H), 7.19 (s, 2H); 13C NMR δ 14.2, 61.6, 118.2, 146.9, 158.1.

References

[1] Patent: WO2016/202858, 2016, A1. Location in patent: Page/Page column 57
[2] Bioorganic and Medicinal Chemistry Letters, 2018,
[3] Patent: WO2012/101015, 2012, A1. Location in patent: Page/Page column 19-20
[4] Polish Journal of Chemistry, 2001, vol. 75, # 12, p. 1943 - 1946
[5] Organic and Biomolecular Chemistry, 2014, vol. 12, # 46, p. 9324 - 9328

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