The Diels–Reese Reaction is a reaction between hydrazobenzene and dimethyl acetylenedicarboxylate (or related esters) first reported in 1934 by Otto Diels and Johannes Reese. Later work by others extended the reaction scope to include substituted hydrazobenzenes. The exact mechanism is not known. By changing the acidic or basic nature of the solvent, the reaction gives different products. With acetic acid as solvent (acidic), the reaction gives an diphenylpyrazolone. With xylene as solvent (neutral), the reaction gives an indole. With pyridine as solvent (basic), the reaction gives a carbomethoxyquinoline which can be degraded to a dihydroquinoline.
References
- Diels, Otto; Reese, Johannes (1934). "Syntheses in the hydroaromatic series. XX. Addition of acetylenedicarboxylic esters to hydrazobenzene". Justus Liebigs Annalen der Chemie. 511: 168–182. doi:10.1002/jlac.19345110114.
- Diels, Otto; Reese, Johannes (1935). "Syntheses in the hydroaromatic series. XXV. Addition products of acetylenedicarboxylic esters and hydrazo compounds. 2". Justus Liebigs Annalen der Chemie. 519: 147–157. doi:10.1002/jlac.19355190113.
- Huntress, Ernest H.; Bornstein, Joseph; Hearon, William (1956). "An Extension of the Diels–Reese Reaction". J. Am. Chem. Soc. 78 (10): 2225–2228. doi:10.1021/ja01591a055.
 | This organic chemistry article is a stub. You can help Misplaced Pages by expanding it. |