- Riehm Quinoline Synthesis
-
Riehm Synthesis
P. Riehm et al., Ber. 18, 2245 (1885); 19, 1394 (1886); idem, Ann. 238, 9 (1887).
Formation of quinoline derivatives by prolonged heating of arylamine hydrochlorides with ketones with or without use of aluminum chloride or phosphorus pentachloride:

E. Knoevenagel et al., Ann. 55, 1923, 1934 (1922); 56, 2414 (1923); C. Hollins, The Synthesis of Ring Compounds (London, 1924) p 263; D. J. Craig, J. Am. Chem. Soc. 60, 1458 (1938); R. C. Elderfield, J. R. McCarthy, ibid. 73, 975 (1951); R. C. Elderfield, Heterocyclic Compounds 4, 16 (1952).
Prev: Riemschneider Thiocarbamate Synthesis
Next: Reverdin Reaction - 【Back】【Close 】【Print】【Add to favorite 】
- Related information
- Production Method of Wy-47288
- Synthesis of PK-9084
- Production Method of Pipequaline
- Synthesis of 4,7-Dichloroquinoline
- Preparation of 4-Methylpyrrolo[1,2-a]quinoline
- Systematic Method of 4,7-Dichloroquinoline
- Preparation of 6-Methoxy-8-nitroquinoline
- Purification of Quinoline
- Pfitzinger Reaction
- Niementowski Quinoline Synthesis
-
Health and Chemical more >
-
Hot Products
- 874-42-0 2,4-Dichlorobenzaldehyde
- 1202044-20-9 Ostarine
- 9016-00-6 Poly(dimethylsiloxane)
- 924661-13-2 1-Silanaphthalene, 1,2,3,4-tetrahydro-1-(1-methylethyl)-, (1R)-
- 1344-09-8 Sodium silicate
- 5593-20-4 Betamethasone 17,21-dipropionate
- 4300-97-4 3-Chloropivaloyl chloride
- 261503-43-9 5,5,6,6,7,7,7-Heptafluoro-4,4-bis(trifluoromethyl)hept-2-enoic acid
- 1343-98-2 Silicic acid
- 68-19-9 Cyanocobalamin
- 75-98-9 Pivalic acid
- 13081-18-0 Ethyl trifluoropyruvate


