Synthesis of 4-ketocyclopentene and cyclopentadiene compounds
AssigneeThe Dow Chemical Company
InventorRavi B. Shankar
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AssigneeThe Dow Chemical Company
InventorRavi B. Shankar
Estimating the term…
A process for forming 4-ketocyclopentene and substituted 4-ketocyclopentene compounds starting from the corresponding 1-carbohydrocarbyloxy-2-keto-4-hydroxy-5-cyclopentene by reduction followed by decarboxylation using zinc dichloride or zinc dibromide. The ketone may thereafter be converted to a cyclopentadiene compound by reducing the ketone to form an alcohol, replacing the hydroxyl functionality of the alcohol under substitution conditions with a leaving group, and deprotonating the resulting product under base induced elimination conditions to form the cyclopentadiene compound. Alternatively functionalized cyclopentadienyl compounds can be produced without isolation of an unsubstituted cyclopentadienyl compound by combining the elimination and deprotonation steps with a replacement step in a single unit operation.
A process for forming a 4-ketocyclopentene compound comprising reducing a 1-carbohydrocarbyloxy-2-keto-4-hydroxy-5-cyclopentene compound by contacting with a metal and decarboxylating the resulting reaction product by contacting with a mixture of an organic acid and an inorganic halide compound selected from the group consisting of zinc dichloride and zinc dibromide.
Dependencies are inferred from the claim text.