The Diels-Reese Reaction was first discovered by O. Diels and J. Reese in 1934. The reaction is believed to carry on by an unknown intermediate or adduct as proposed by Hearon. By varying the solvent the resultant product will change. With acetic acid as solvent (acidic pH), the reaction gives the diphenylpyrazolone. With xylene as solvent (neutral pH), the reaction yields the indole, and with pyridine (basic pH), the reaction gives the carbomethoxyquinoline which can then be degraded to the dihydroquinoline.
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