Coupling of o-tolidine and chicago acid
CAS index name: Preparation of a Salt-Free Azo Dye
Organic SynthesesCross-coupling
A checked procedure from Organic Syntheses, the journal whose preparations are repeated in a second laboratory before publication. The full experimental, with amounts, hazards and characterisation data, is on orgsyn.org.
Reagents
The compound this preparation makes is not in the catalogue, so no reagents or figures are listed here.
More cross-coupling reactions
- Accelerated Suzuki coupling via a ligandless palladium catalyst: 4-methoxy-2'-methylbiphenyl
- Alkynyl(phenyl)iodonium tosylates: preparation and stereospecific coupling with vinylcopper reagents. Formation of conjugated enynes. 1-Hexynyl(phenyl)iodonium tosylate and (E)-5-phenyldodec-5-en-7-yne
- Discussion addendum for: 4-methoxy-4'-nitrophenyl. Recent advances in the Stille biaryl coupling reaction and applications in complex natural products synthesis
- Discussion Addendum for: palladium catalyzed cross-coupling of (Z)-1-heptenyldimethylsilanol with 4-iodoanisole: (Z)-(1-heptenyl)-4-methoxybenzene
- Discussion Addendum for: Suzuki-Miyaura Cross-Coupling: Preparation of 2'-Vinylacetanilide
- Discussion Addendum for: Synthesis of 4-, 5-, and 6-Methyl-2,2'-Bipyridine by a Negishi Cross-Coupling Strategy: 5-Methyl-2,2'-Bipyridine