Synthesis of furan derivatives using the reaction of 1,3-dicarbonyl compounds with various α-haloketones
The reaction of 1,3-dicarbonyl compounds with ethyl bromopyruvate thus led to dihydrofurans in good yields. Dihydrofurans were converted to the corresponding furan derivatives in the presence of p-toluenesulfonic acid (p-TSA). While, the reaction of phenacyl bromides with 1, 3-dicarbonyl compounds led to either esters or α-substituted acetophenones in moderate yields.
Authors
- IAU
Publication Details
- Published
- 2025-12-24
- DOI
- https://doi.org/10.82361/iranjoc.2025.1229260
- Primary Topic
- Organic Chemistry Synthesis Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00