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HRID 72814作成日:2026年10月26日

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

https://huagongshe.com/reaction/72814

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromotolueneHCID 7236—
反応物2-ChlorotolueneHCID 7238—
反応物Lithium amideHCID 24532—
反応物2-(Di-tert-butylphosphino)biphenylHCID 2734215—
反応物Sodium t-butoxideHCID 23676156—
触媒(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
溶媒Diethyl EtherHCID 3283—
生成物Benzenamine, 2-methyl-N-(2-methylphenyl)-HCID 13642372%

反応手順

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)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08828986B2
出典データセットuspto-grants-2014_09
ORD IDord-6dc0c40063fa4ce2bed62a222591a84e
出典メモuspto-grants-2014_09