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Pyridinium dichromate acts as a strong oxidizing agent used in the conversion of primary alcohols and secondary alcohols to aldehydes and ketones respectively. It plays an important role in the oxidation of unsaturated tertiary alcohols, silyl ethers, the carbon-boron bond, and oximes. Further, it is used in the conversion of acetals to esters and didehydroketones to enones in the presence of tert-butyl hydroperoxide.
Selective oxidant which can be used in dichloromethane to convert primary alcohols to aldehydes: Tetrahedron Lett., 399 (1979). Can also be used catalytically in combination with Sodium percarbonate, A16045, as co-oxidant for conversion of allylic and benzylic alcohols to aldehydes under phase-transfer conditions: Tetrahedron Lett., 35, 1989 (1994). Under the same conditions, ɑ-functionalized benzylic alcohols undergo oxidative cleavage: Synth. Commun., 25, 2051 (1995).
Matsunaga, K.; Hirajima, H.; Kishida, A.; Takatori, K.; Nagaoka, H. Novel PDC catalyzed oxidative rearrangement of tertiary allylic alcohols to beta-substituted enones. Tetrahedron Lett. 2015, 56 (43), 5941-5944.
Ghosh, A.; Saha, R.; Mukherjee, K.; Ghosh, S. K.; Sar, P.; Malik, S.; Saha, B. Choice of suitable micellar catalyst for 2,2'-bipyridine-promoted chromic acid oxidation of glycerol to glyceraldehyde in aqueous media at room temperature. Res. Chem. Intermed. 2015, 41 (5), 3057-3078.
Gefahrenhinweise (EU): H272-H314-H317-H351
May intensify fire; oxidizer. Causes severe skin burns and eye damage. May cause an allergic skin reaction. Suspected of causing cancer.
Take any precaution to avoid mixing with combustibles. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.