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Dimethyl Furan-2,5-dicarboxylate

Dimethyl  Furan-2,5-dicarboxylate Structure
CAS No.
4282-32-0
Chemical Name:
Dimethyl Furan-2,5-dicarboxylate
Synonyms
dimethyl furan-2,5-dicarboxylate;Dimethyl 2,5-furandic;2,5-Bis(methoxycarbonyl)furan;Methyl Furan-2,5-dicarboxylate;Dimethyl 2,5-furandicarboxylate;Dimethy Furan-2,5-dicarboxylate;Dimethyl furan dicarboxylic acid;2,5-Dimethyl 2,5-furandicarboxylate;Dimethyl furan-2,5-dicarboxylate 99%;DimethylFuran2,5-Dicarboxylate (FDCAE)
CBNumber:
CB82130468
Molecular Formula:
C8H8O5
Molecular Weight:
184.15
MOL File:
4282-32-0.mol
MSDS File:
SDS
Modify Date:
2024/8/12 17:17:06

Dimethyl Furan-2,5-dicarboxylate Properties

Melting point 112°C
Boiling point 278.08°C (rough estimate)
Density 1.3840 (rough estimate)
refractive index 1.5690 (estimate)
storage temp. 2-8°C
form crystals
color White

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H319-H335-H302+H312+H332-H315
Precautionary statements  P261-P271-P280
HazardClass  IRRITANT
HS Code  2918999090

Dimethyl Furan-2,5-dicarboxylate Chemical Properties,Uses,Production

Description

Dimethyl Furan-2,5-dicarboxylate is a structural analog of diacids. It has been synthesized by the reaction of 5-hydroxymethylfurfural with ethyl esters and phosphotungstic acid.

Uses

2,5-Furandicarboxylic acid dimethyl ester can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development processes and chemical production processes.

Synthesis

Synthesis_4282-32-0Preparation of dimethyl FDCA from methyl 5-formyl-2- furoate: A 15 niL glass liner was charged with a magnetic stirring bar, methyl 5- formyl-2-furoate (117 mg, 0.76 mmol), methanol (10 mL) and sodium methoxide (4 mg, 0.076 mmol) to give a clear solution. A 1.2 wt% Au/Ti02 (41.5 mg, 2.53 |ì|é|?|? Au) catalyst was added to give a purple suspension and the vial was placed in a 75 mL Parr Hastelloy C-276 reactor. The reactor was closed and flushed 3x with compressed air and then pressurized at 4.6 bar. Stirring was started (600 rpm) and the reaction was allowed to proceed at room temperature. After 19 h, the reaction had consumed 0.25 bar of air and the reactor was opened. The reaction mixture was filtered over Celite to remove the catalyst, which was washed with a httle methanol and dichlorom ethane. The combined organic layers were washed with water, dried over MgS04, filtered, and the solvent was removed under reduced pressure. 2,5-FDCA dimethyl ester was obtained as light yellow crystals (106 mg, yield 76%).

Dimethyl Furan-2,5-dicarboxylate Preparation Products And Raw materials

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2,5-Furandicarboxylic acid dimethyl ester Furan-2,5-dicarboxylic acid dimethyl ester Methyl Furan-2,5-dicarboxylate 2,5-Bis(methoxycarbonyl)furan Dimethyl 2,5-furandicarboxylate Dimethyl furan dicarboxylic acid Dimethyl furan-2,5-dicarboxylate 99% Dimethyl 2,5-furandic 2,5-Furandicarboxylic acid, 2,5-dimethyl ester Dimethy Furan-2,5-dicarboxylate dimethyl furan-2,5-dicarboxylate 2,5-Dimethyl 2,5-furandicarboxylate DimethylFuran2,5-Dicarboxylate (FDCAE) 2, 5- Furandicarboxylicacid dimethyl ester(FDME) 4282-32-0 4280-32-0 4282-32-0