Related Experiment Video
Updated: Nov 11, 2025

Temperature-programmed Deoxygenation of Acetic Acid on Molybdenum Carbide Catalysts
Published on: February 7, 2017
Mild Condition for the Deoxygenation of α-Heteroaryl-Substituted Methanol Derivatives
Na Meng1, Wensheng Yu2, Takao Suzuki1
1IDSU, WuXi AppTec Company, Ltd., Shanghai 200131, China.
Abstract:
A mild condition via PPh3/I2/imidazole for the deoxygenation of substituted methanol derivatives has been identified. This metal-free process was found to proceed well on secondary or tertiary alcohols substituted with one or two heteroaryl groups, and it tolerates acid-sensitive heterocycles. This condition works for methanol derivatives substituted with 2-pyridyl, 4-pyridyl, or other heterocyclic groups, allowing the negative charge formed during the reaction to resonate to a nitrogen atom. Methanol derivatives substituted with 3-pyridyl or heterocyclic groups that do not allow the negative charge formed during the reaction to resonate to a nitrogen atom will not undergo deoxygenation under this condition.
Related Concept Videos
ortho–para-Directing Activators: –CH3, –OH, –⁠NH2, –OCH3
Oxidation of Alcohols
The process of oxidation in a chemical reaction is observed in any of the three forms:
Preparation of Aldehydes and Ketones from Alcohols, Alkenes, and Alkynes
Acid-Catalyzed Dehydration of Alcohols to Alkenes
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Hydroboration-Oxidation of Alkenes

