Friedel-crafts acylation process in ionic liquids
View Patent ↗A preparation process of aromatic ketones by a Friedel-Crafts acylation reaction in an ionic liquid of formula (I), in the absence of any other catalyst and/or solvent. In formula (I), [Q] + is selected from substituted-imidazolium cations, substituted-pyridinium cations, ammonium cations, and phosponium cations. It allows to carry out Friedel-Crafts acylations with good yields and high selectivity in para position of the Friedel-Crafts aromatic substrate without using chlorine-containing solvents and conventional Friedel-Crafts catalysts. It is industrially useful because provides a “Green Chemistry” technology for carrying out Friedel-Crafts acylations of general aplicability. [Q] + [CF 3 SO 3 ] − (I)
1. A process for preparation of aromatic ketones by a Friedel-Crafts acylation reaction in an ionic liquid, between a Friedel-Crafts aromatic substrate and a Friedel-Crafts acylating agent, wherein the ionic liquid has the formula (I) and is used in the absence of any other catalyst and/or solvent; wherein [Q] + is selected from the group consisting of a substituted-imidazolium cation, a substituted-pyridinium cation, an ammonium cation, and a phosponium cation.
[Q] + [CF 3 SO 3 ] − (I)
2. The process according to claim 1 , wherein [Q] + is a substituted-imidazolium cation.
3. The process according to claim 2 , wherein the ionic liquid is selected from the group consisting of 1-ethyl-3-methylimidazolium trifluoromethanesulfonate, 1,3-diethylimidazolium trifluoromethanesulfonate, and 1,3-dimethylimidazolium trifluoromethanesulfonate.
4. The process according to claim 3 , wherein the ionic liquid is 1-ethyl-3-methylimidazolium trifluoromethanesulfonate.
5. The process according to claim 1 , wherein the Friedel-Crafts acylating agent is selected from the group consisting of a carboxylic acid halide, a carboxylic acid anhydride, a carboxylic acid ester and a carboxylic acid.
6. The process according to claim 5 , wherein the Friedel-Crafts acylating agent is a carboxylic acid anhydride.
7. The process according to claims 5 , wherein the acylating agent is selected from the group consisting of acetic acid anhydride, propionoic acid anhydride, butanoic acid anhydride, isobutanoic acid anhydride, pentanoic acid anhydride, benzoic acid anhydride, chloroacetic acid anhydride, acetyl chloride, propanoyl chloride, butanoyl chloride, benzoyl chloride, and chloroacetyl chloride.
8. The process according to claim 1 , wherein the Friedel-Crafts aromatic substrate is selected from the group consisting of aromatic benzenoid compounds, aromatic benzenoid-fused compounds, and heteroaromatic compounds resulting from substitution of CH groups by N atoms in said aromatic benzenoid compounds and aromatic benezenoid-fused compounds; said aromatic and heteroaromatic substrates being optionally substituted by substituents which are stable under Friedel-Crafts reaction conditions, or which have been suitably protected to be stable.
9. The process according to claim 8 , wherein the Friedel-Crafts aromatic substrate is selected from the group consisting of benzene, toluene and anisole.
10. The process according to claim 9 , wherein the Friedel-Crafts aromatic substrate is anisole.
11. The process according to claim 1 , wherein the Friedel-Crafts acylating agent is attached to the Friedel-Crafts aromatic substrate, the carbonyl group of the Friedel-Crafts acylating agent being separated from the Friedel-Crafts aromatic substrate by a aliphatic chain from 2 to 4 carbon atoms, effecting an intramolecular ring closure and yielding a (5-7)-membered ring.
12. The process according to any one of claims 1 - 6 and 8 - 9 , wherein the reaction is carried out at a temperature between room temperature and 150° C.
13. The process according to any one of claims 1 - 6 and 8 - 9 , wherein the reaction is carried out at a temperature between 70° C. and 100° C.
14. The process according to claim 6 , wherein the acylating agent is selected from the group consisting of acetic acid anhydride, propionoic acid anhydride, butanoic acid anhydride, isobutanoic acid anhydride, pentanoic anhydride, benzoic acid anhydride, chloroacetic acid anhydride, acetyl chloride, propanoyl chloride, butanoyl chloride, benzoyl chloride, and chloroacetyl chloride.
15. The process according to claim 1 , wherein the ionic liquid is used in the absence of any other catalyst and solvent.
16. The process according to claim 14 , wherein the reaction is carried out at a temperature between room temperature and 150° C.