Achmatowicz Reaction Mechanism | Organic Chemistry @OrganicMechanismsChannel
Achmatowicz Reaction Mechanism | Organic Chemistry  @OrganicMechanismsChannel
Uploaded September 2021 | Updated September 2026, 1 week ago
The mechanism for a Achmatowicz reaction in which a furan is converted to a dihydropyran. The furan is first reacted with bromine in methanol which then goes through a rearrangement. An acid is then required to complete the reaction, often sulfuric acid is used in this reaction. In place of bromine, m-CPBA can also be used in order to accomplish this synthesis.

Music: Freefall – YouTube Audio Library
Achmatowicz Reaction Mechanism | Organic ChemistryWacker Oxidation Mechanism | Organic ChemistryTES Protecting Group Addition With TESOTf | Organic ChemistryCDTP Peptide Coupling Mechanism | Organic ChemistryMukaiyama Aldol Reaction Mechanism | Organic ChemistryBouveault Aldehyde Synthesis Mechanism | Organic ChemistryCannizzaro Reaction Mechanism | Organic ChemistryBTFFH Peptide Coupling Mechanism | Organic ChemistryGomberg-Bachmann Reaction Mechanism | Organic ChemistrySodium Dithionite Reduction Mechanism | Organic ChemistryUsing Cyanuric Chloride To Produce HCl Mechanism | Organic ChemistrySodium Periodate Oxidation Mechanism | Organic Chemistry
Organic Mechanisms |

Achmatowicz Reaction Mechanism | Organic Chemistry

SHARE TO X SHARE TO REDDIT SHARE TO FACEBOOK WALLPAPER