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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 72814Erstellt: 25. Oktober 2026

2-Bromotoluene → Benzenamine, 2-methyl-N-(2-methylphenyl)-

https://huagongshe.com/reaction/72814

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromotolueneHCID 7236—
Edukt2-ChlorotolueneHCID 7238—
EduktLithium amideHCID 24532—
Edukt2-(Di-tert-butylphosphino)biphenylHCID 2734215—
EduktSodium t-butoxideHCID 23676156—
Katalysator(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTolueneHCID 1140—
LösungsmittelDiethyl EtherHCID 3283—
ProduktBenzenamine, 2-methyl-N-(2-methylphenyl)-HCID 13642372%

Reaktionsschritte

The round-bottom flask was heated then allow to cool to room temperature under argon. Added Pd2(dba)3 (1.39 g, 1.52 mmol, 1.0 mol %) or Pd(dba)2 (1.38 g, 2.4 mmol, 1.4 mol %), 2-(di-tert-butylphosphino)biphenyl (1.09 g, 3.65 mmol, 2.4 mol %), 2-bromotoluene (40 mL, 332.1 mmol) or 2-chlorotoluene (39 mL, 332.1 mmol), lithium amide (3.47 g, 151.1 mmol, 45 mol %), sodium t-butoxide (29.5 g, 297.7 mmol, 90 mol %), followed by toluene (150 mL). The reaction mixture was heated at 80° C. under argon overnight, then allowed to cool to room temperature. Diluted with diethyl ether then filtered through a pad of Celite. Concentrated the resulting filtrate in vacuo. Used the crude material in the next reaction without purification. (Crude material can be purified by flash chromatography with hexane which gave the product as white crystals with a yellow tint (23.4 g, 118.6 mmol, 72% yield)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08828986B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-6dc0c40063fa4ce2bed62a222591a84e
Quellennotizuspto-grants-2014_09