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Usage

Uses

Used in Flavor and Fragrance Industry:
2-(furan-2-yl)-4,5-dimethyl-1,3-dioxolane is used as a flavor and fragrance ingredient for its sweet, caramel-like aroma, enhancing the sensory experience of various products.
Used in Chemical Production:
In the chemical industry, 2-(furan-2-yl)-4,5-dimethyl-1,3-dioxolane serves as a key component in the production of resins and adhesives, contributing to the development of durable and versatile materials.
Used in Pharmaceutical Industry:
As a starting material in the pharmaceutical sector, 2-(furan-2-yl)-4,5-dimethyl-1,3-dioxolane is utilized for synthesizing other compounds, playing a crucial role in the creation of new medications and therapeutic agents.

Upstream product

• 98-01-1 furfural 
• 24347-58-8 (R,R)-2,3-butandiol 

Relevant academic research and scientific papers

Torii-Type Electrosynthesis of α,β-Unsaturated Esters from Furfurylated Ethylene Glycols and Amino Alcohols

Electrosynthesis of unsaturated esters from furan derivatives, reported by Torii et al. in 1976, is an attractive method for the valorization of furanoic platform chemicals. Nevertheless, it has received practically no attention, presumably due to specific reaction conditions including the use of expensive Pt electrodes. With the aim of expanding the application of Torii-type ester electrosynthesis, we explored the electrochemical transformation of O-furfuryl ethylene glycols and N-furfuryl amino alcohols to esters 5. These can be obtained in two consecutive electrochemical steps: bis-alkoxylation of the furan derived substrates 3 to give spirocycles 4, followed by ring-opening involving oxidative fragmentation of the C?C bond. Both steps can be carried out at ambient conditions, using inexpensive graphite electrodes; however, each step required a different supporting electrolyte and acidic additive to achieve good yields of the product. Additionally, conditions were found for efficient one-pot transformation of N-furfuryl amino alcohols to esters 5 while O-furfuryl ethylene glycols under the same conditions gave esters 5 in moderate yields.

Enantiomerically pure Diels-Alder adducts of maleic anhydride to furfural acetals through thermodynamic control. Single crystal and molecular structure of (1S,4R,4'S,5'S)-1-(4',5'-dimethyldioxolan-2'-yl)-5,6-dimethylidene-7-o xabicyclo[2.2.1]hept-2-ene

The acetal of (2S,3S)-butane-2,3-diol and furfural is equilibrated in molten maleic anhydride with one major crystalline product which is a 1:1 complex of maleic anhydride and (1S,2R,3S,4R,4'S,5'S)-1-(4',5'-dimethyldioxolan-2'-yl)-7-oxabicyclo[2. 2.1]hept-5-ene-2-exo,3-exo-dicarboxylic anhydride. This compound was converted into (1S,4R,4'S,5'S)-1-(4',5'-dimethyldioxolan-2'-yl)-5,6-dimethylidene-7-o xabicyclo[2.2.1]hept-2-ene (+)-12, the circular dichroism spectrum of which suggests a slightly skew s-cis-butadiene chromophore as confirmed by X-ray diffraction. Copyright (C) Elsevier Science Ltd.