Abstract
Nucleophilic aromatic substitution of hydrogen in non-activated aromatic ring, a very rare phenomenon in organic chemistry, is found in ionic liquids containing Cl- as anion under mild reaction conditions. The reaction may be carried out by the addition of the halogen-bonding adduct (Br 2Cl-) as nucleophile to aromatic ring carbon atom, leading to the formation of the nucleophilic substitution product.
| Original language | English |
|---|---|
| Pages (from-to) | 147-150 |
| Number of pages | 4 |
| Journal | Chinese Chemical Letters |
| Volume | 22 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 2011 |
Keywords
- Aromatic compound
- Halogen bonding
- Ionic liquid
- Naphthalene
- Nucleophilic reaction
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