- Chichibabin Pyridine Synthesis
-
Chichibabin Synthesis
A. E. Chichibabin, J. Russ. Phys. Chem. Soc. 37, 1229 (1906); J. Prakt. Chem. 107, 122 (1924).
Condensation of carbonyl compounds with ammonia or amines under pressure to form pyridine derivatives; the reaction is reversible and produces different pyridine derivatives along with byproducts:

M. M. Sprung, Chem. Rev. 26, 301 (1940); R. L. Frank, R. P. Seven, J. Am. Chem. Soc. 71, 2629 (1949); H. S. Mosher, Heterocyclic Compounds 1, 456 (1950); J. A. Gautier, J. Renault, Bull. Soc. Chim. France 1955, 588; C. P. Farley, E. L. Eliel, J. Am. Chem. Soc. 78, 3477 (1956); A. T. Soldatenkov, Zh. Org. Khim. 16, 188 (1980). Cf. Hantzsch (Dihydro)Pyridine Synthesis; Kröhnke Pyridine Synthesis.
Prev: Chichibabin Reaction
Next: Chapman Rearrangement - 【Back】【Close 】【Print】【Add to favorite 】
- Related information
- International Priceso of Synthesis Ammonia in the Falling Trends
- International Prices of Synthesis Ammonia in Falling Trends
- International Prices of Synthesis Ammonia in Falling Trends
- International Prices of Synthesis Ammonia in Differentiation Trends
- International Prices of Synthesis Ammonia in Differentiation Trends
- International Prices of Synthesis Ammonia in Rising Trend
- International Prices of Synthesis Ammonia in Rising Trend
- International Prices of Synthesis Ammonia in Rising Trend
- International Prices of Synthesis Ammonia in Rising Trend
- International Prices of Synthesis Ammonia in Early September
-
Health and Chemical more >
-
Hot Products
- 7663-51-6 6a,7,8,9-Tetrahydro-6,6,9-trimethyl-3-pentyl-6H-dibenzo[b,d]pyran-1-ol
- 75-65-0 tert-Butyl alcohol
- 8007-18-9 C. I. Pigment Yellow 53 (77788)
- 16872-11-0 Fluoroboric acid
- 2398-96-1 Tolnaftate
- 131543-23-2 WIN 55212-2 mesylate
- 50691-09-3 5-oxo-3-(4-phenylphenyl)-2H-furan-4-carbonitrile
- 616202-92-7 Lorcaserin
- 12037-01-3 Tetraterbium heptaoxide
- 82957-06-0 6-Amidino-2-naphthol methanesulfonate
- 148-79-8 Thiabendazole
- 7790-38-7 PALLADIUM(II) IODIDE


