Abstract: The present disclosure provides a process for regenerating the deactivated ionic compound. The process involves mixing a deactivated ionic compound with at least one solvent such as ethyl acetate and neutralizing with at least one base such as triethylamine and tert-butyl amine to obtain a precipitate. The obtained precipitate is filtered to obtain a residue which is then washed with a solvent such as dichloromethane to obtain the ionic compound.

Abstract: The present disclosure provides an ionic liquid compound of Formula (I) and its application in reactions such as alkylation, arylation, acylation, diels alder and oligomerization, The present disclosure also provides a process for preparing the ionic liquid compound of Formula (I) which involves preparing an ionic salt complex represented by Formula [(NR1R2R3)iM1]n+[Xj]n? by mixing an amine represented by Formula NR1R2R3 and a metal salt represented by formula M1Xj; and mixing the ionic salt complex and a metal salt represented by formula M2Yk to obtain the ionic liquid compound.

Abstract: In the present disclosure, a process for separating aryl carboxylic acids from a mixture comprising a plurality of aryl carboxylic acids is provided, wherein the process comprising the steps of heating a first mixture that comprises at least two aryl carboxylic acids wherein each of said aryl carboxylic acids having a pre-determined liquefaction temperature and a pre-determined precipitation temperature, with at least one ionic compound, at a pre-determined temperature to obtain a liquefied composition; and cooling the liquefied composition under controlled temperature conditions to fractionally crystallize and precipitate an aryl carboxylic acid. The precipitated aryl carboxylic acid is isolated and the obtained mother liquor is subjected to iterated cooling steps until each of the remaining aryl carboxylic acids precipitates one by one. The mother liquor remains in liquefied form.

Abstract: A process for preparing alditol Acetals via a dehydrocondensation reaction is disclosed. The reaction is carried out by adding an aldehyde and an aldiol using a metal salt based ionic liquid as an acid catalyst. The ionic liquid used in the process is prepared by dissolving a hydrogen donor and a compound providing counter ion in a solvent.

Abstract: A process for the preparation of 1,3:2,4-bis(4-methylbenzylidene)sorbitol (MDBS) and 1,3:2,4-bis(3,4-dimethylbenzylidene)sorbitol (DMDBS) via a dehydrocondensation reaction is disclosed. The reaction is carried out between an aldehyde and an alditol in a mole ratio of 2:1 wherein ionic fluid is used as the acidic catalyst and/or reaction medium. The ionic fluid used in accordance with the present invention is quaternary ammonium salt based ionic liquid.

Abstract: In the present disclosure, a process for separating aryl carboxylic acids from a mixture comprising a plurality of aryl carboxylic acids is provided, wherein the process comprising the steps of heating a first mixture that comprises at least two aryl carboxylic acids wherein each of said aryl carboxylic acids having a pre-determined liquefaction temperature and a pre-determined precipitation temperature, with at least one ionic compound, at a pre-determined temperature to obtain a liquefied composition; and cooling the liquefied composition under controlled temperature conditions to fractionally crystallize and precipitate an aryl carboxylic acid. The precipitated aryl carboxylic acid is isolated and the obtained mother liquor is subjected to iterated cooling steps until each of the remaining aryl carboxylic acids precipitates one by one. The mother liquor remains in liquefied form.

Abstract: This invention is directed to a process for preparation of acetal derivatives, 1,3:2,4-bis(3,4-dimethylbenzylidene)sorbitol (DMDBS) and 1,3:2,4-bis(4-methylbenzylidene)sorbitol (MDBS) by carrying out a dehydrocondensation reaction between an aldehyde and an alditol using an aqueous ionic fluid as the acid catalyst.

Abstract: The present invention is directed to a process for the preparation of 1,3:2,4-bis (4-methylbenzylidene) sorbitol (MDBS) and 1,3:2,4-bis (4-dimethylbenzylidene) sorbitol (DMDBS) by dehydrocondensating an aldehyde and an alditol using a hydrophobic ionic liquid as an acid catalyst. The ionic liquid used in the accordance with the process of the present invention is a phosphonium ion based ionic liquid.

Abstract: A process for preparing alditol Acetals via a dehydrocondensation reaction is disclosed. The reaction is carried out by adding an aldehyde and an aldiol using a metal salt based ionic liquid as an acid catalyst. The ionic liquid used in the process is prepared by dissolving a hydrogen donor and a compound providing counter ion in a solvent.

Abstract: The present invention is directed to a process for the preparation of 1,3:2,4-bis (4-methylbenzylidene) sorbitol (MDBS) and 1,3:2,4-bis (4-dimethylbenzylidene) sorbitol (DMDBS) by dehydrocondensating an aldehyde and an alditol using a hydrophobic ionic liquid as an acid catalyst. The ionic liquid used in the accordance with the process of the present invention is a phosphonium ion based ionic liquid.

Abstract: A process for the preparation of 1,3:2,4-bis (4-methylbenzylidene) sorbitol (MDBS) and 1,3:2,4-bis (3,4-dimethylbenzylidene) sorbitol (DMDBS) via a dehydrocondensation reaction is disclosed. The reaction is carried out between an aldehyde and an alditol in a mole ratio of 2:1 wherein ionic fluid is used as the acidic catalyst and/or reaction medium. The ionic fluid used in accordance with the present invention is quaternary ammonium salt based ionic liquid.

Abstract: This invention is directed to a process for preparation of acetal derivatives, 1,3:2,4-bis (3,4-dimethylbenzylidene)sorbitol (DMDBS) and 1,3:2,4-bis (4-methylbenzylidene)sorbitol (MDBS) by carrying out a dehydrocondensation reaction between an aldehyde and an alditol using an aqueous ionic fluid as the acid catalyst.