4.4 Article

Sulfuric Acid Catalyzed Rapid Nucleophilic Substitution of Propargyl Alcohols

Journal

CHINESE JOURNAL OF ORGANIC CHEMISTRY
Volume 40, Issue 5, Pages 1257-1265

Publisher

SCIENCE PRESS
DOI: 10.6023/cjoc201911036

Keywords

sulfuric acid; catalyzed; propargyl alcohols; nucleophilic substitution

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Sulfuric acid efficiently catalyzes the direct substitution of the hydroxyl group of propargylic alcohols with a variety of C- and O-based nucleophiles to aid C-C and C-O bond formation. The reactions can be performed in an undried solvent under air atmosphere to obtain the desired products in good yields. In most cases, the reaction proceeds to completion in 1 min at room temperature.

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