Oxidation of benzylic alcohols to their corresponding carbonyl compounds using ceric ammonium nitrate (CAN)/bronsted acidic ionic liquid was written by Hajipour, A. R.;Khazdooz, L.;Ruoho, A. E.. And the article was included in Journal of the Iranian Chemical Society in 2011.Synthetic Route of C10H20N2O4S The following contents are mentioned in the article:
A chemoselective and efficient procedure for the oxidation of alcs. to the corresponding carbonyl compounds is reported using ceric ammonium nitrate in the presence of 3-hexyl-1-methylimidazolium hydrogen sulfate as Bronsted acidic ionic liquid ([Hmim]HSO4) as the solvent under mild conditions. The use of non-toxic and inexpensive materials, straightforward procedure, short reaction times and good yields of the products are the major advantages of this method. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Synthetic Route of C10H20N2O4S).
1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Imidazole based anticancer drug find applications in cancer chemotherapy. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC).Synthetic Route of C10H20N2O4S
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem