Abstract
Furoin was synthesized with furfural as raw material in the presence of Vitamin B1 (VB1) as a catalyst. The monoesters of furoin were synthesized by esterification of corresponding the acyl chloride with the furoin. The new 2-substituted-4,5-di(α-furyl)oxazoles were obtained via treatment of the monoesters with ammonium acetate and acetic acid, characterized with elemental analysis, IR, 1H NMR, mass spectra, and their luminescence property was simply studied with UV and fluorescence spectra.
Original language | English |
---|---|
Pages (from-to) | 1611-1615 |
Number of pages | 5 |
Journal | Chinese Journal of Organic Chemistry |
Volume | 28 |
Issue number | 9 |
Publication status | Published - Sept 2008 |
Externally published | Yes |
ASJC Scopus Subject Areas
- Organic Chemistry
Keywords
- 2-substituted-4,5-di(α-furyl)oxazole
- Esterification
- Furoin
- Luminescent property
- Monoester of furoin
- Synthesis