One-pot synthesis of polyfunctionalized pyrans catalyzed by basic ionic liquid in aqueous media
✍ Scribed by Kai Gong; Hua-Lan Wang; Jun Luo; Zu-Liang Liu
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2009
- Tongue
- English
- Weight
- 78 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.193
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
magnified image An efficient and convenient method for the synthesis of polyfunctionalized 4__H__‐pyrans has been achieved through the one‐pot condensation of aromatic aldehydes, malononitrile, and 4‐hydroxycoumarin, phenols or active methylene carbonyl compounds such as 1, 3‐cyclohexanedione and dimedone in the presence of 1‐butyl‐3‐methyl imidazolium hydroxide ([bmim]OH) as catalyst in aqueous media. This method offers several advantages short reaction time, high yields, and simple procedure. J. Heterocyclic Chem., (2009).
📜 SIMILAR VOLUMES
## Abstract magnified image Some halogen‐free acyclic task‐specific ionic liquids (TSILs) were synthesized as novel and recyclable catalysts for the synthesis of 5‐oxo‐5,6,7,8‐tetrahydro‐4H‐benzo[b]pyrans by one‐pot three‐component condensation of aromatic aldehyde, malononitrile (or ethyl cyanoac