Abstract
The photo-Friedel-Crafts acylation of 1,4-naphthoquinone with various aldehydes was investigated in a series of room temperature ionic liquids. High conversions and selectivities were achieved in [C2mim] +-based ionic liquids with the highest isolated yields found in [C2mim][NTf2]. The developed procedure allowed for a replacement of hazardous solvents such as benzene and acetonitrile which are commonly used for this transformation.
Original language | English |
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Pages (from-to) | 1867-1870 |
Number of pages | 4 |
Journal | Green Chemistry |
Volume | 11 |
Issue number | 11 |
DOIs | |
Publication status | Published - 2009 |