One-pot synthesis of 2-aminobenzothiazoles using a new reagent of [bmim]br3 in [bmim]BF4
✍ Scribed by Zhang-Gao Le; Jian-Ping Xu; Huo-Yu Rao; Min Ying
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2006
- Tongue
- English
- Weight
- 41 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
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The one‐pot direct synthesis of 2‐aminobenzothiazoles from phenyl isothiocyanate and amines using a new reagent of 1‐butyl‐3‐methylimidazolium tribromide ([Bmim]Br~3~) in ionic liquid 1‐butyl‐3‐methylimidazolium tetraflouoroborate ([Bmim]BF~4~) is described.
📜 SIMILAR VOLUMES
## Abstract The one‐pot three component condensation of hydrazine hydrate with substituted phenylisothiocyanates followed by the addition of substituted benzaldehydes in the presence of ionic liquid 1‐butyl‐3‐methylimidazolium tetrafluoroborate ([bmim]BF~4~) and in the absence of any other catalyst