The Feist–Benary synthesis is an organic reaction between α-halo ketones and β-dicarbonyl compounds to produce substituted furan compounds. This condensation...
3 KB (261 words) - 23:56, 11 September 2023
Furan (section Synthesis of furans)
pentose-containing materials, and cellulosic solids, especially pine wood. The Feist–Benary synthesis is a classic way to synthesize furans. The reaction involves alkylation...
18 KB (1,468 words) - 16:08, 10 June 2024
Hantzsch pyrrole synthesis Knorr pyrrole synthesis Feist–Benary synthesis Volhard–Erdmann cyclization Hantzsch pyridine synthesis Paal, C. (1884), "Ueber...
15 KB (1,628 words) - 14:29, 8 June 2024
carbazole synthesis Danheiser annulation Dieckmann condensation Diels–Alder reaction Feist–Benary synthesis Fiesselmann thiophene synthesis Fischer indole...
2 KB (277 words) - 13:03, 12 October 2024
Chloroacetone (section Synthesis)
intermediate in chemical manufacturing. It is also used in the Feist-Benary synthesis of furans. Reaction of phenoxide with chloroacetone gives phenoxyacetone...
6 KB (380 words) - 12:19, 27 June 2024
2,3-Dihydrofuran (section Synthesis and occurrence)
versatile intermediate. 2,3-Dihydrofurans are intermediates in the Feist–Benary synthesis of furans from α-halogen ketones and β-dicarbonyl compounds. The...
4 KB (358 words) - 15:54, 3 March 2024
Knoevenagel condensation (redirect from Doebner synthesis)
aldehyde or ketone. The Hantzsch pyridine synthesis, the Gewald reaction and the Feist–Benary furan synthesis all contain a Knoevenagel reaction step....
7 KB (729 words) - 15:22, 28 August 2024
reaction Favorskii rearrangement Favorskii–Babayan synthesis Fehling test Feist–Benary synthesis Fenton reaction Ferrario reaction Ferrier carbocyclization...
37 KB (3,419 words) - 11:08, 19 October 2024