ChemicalBook--->CAS DataBase List--->53662-83-2

53662-83-2

53662-83-2 Structure

53662-83-2 Structure
IdentificationBack Directory
[Name]

2,5-FURANDICARBOXYLIC ACID DIETHYL ESTER
[CAS]

53662-83-2
[Synonyms]

Diethyl 2,5-furandicarboxylate
Diethyl furan-2,5-dicarboxylate
Diethyl furan-2,5-dicarboxylate 99%
2,5-FURANDICARBOXYLIC ACID DIETHYL ESTER
Furan-2,5-dicarboxylic Acid Diethyl Ester
2,5-Furandicarboxylic acid, 2,5-diethyl ester
[Molecular Formula]

C10H12O5
[MDL Number]

MFCD00449457
[MOL File]

53662-83-2.mol
[Molecular Weight]

212.199
Chemical PropertiesBack Directory
[Melting point ]

46-48°C
[Boiling point ]

167-1680C/15Torr
[density ]

1.172±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

White
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2932190090
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Uses]

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

2,5-Furandicarboxylic acid

3238-40-2

Ethanol

64-17-5

2,5-FURANDICARBOXYLIC ACID DIETHYL ESTER

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
Spectrum DetailBack Directory
[Spectrum Detail]

2,5-FURANDICARBOXYLIC ACID DIETHYL ESTER(53662-83-2)MS
2,5-FURANDICARBOXYLIC ACID DIETHYL ESTER(53662-83-2)1HNMR
2,5-FURANDICARBOXYLIC ACID DIETHYL ESTER(53662-83-2)IR1
2,5-FURANDICARBOXYLIC ACID DIETHYL ESTER(53662-83-2)IR2
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