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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72814생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/72814

반응식

참여 물질

역할이름HCID투입량
반응물2-BromotolueneHCID 7236—
반응물2-ChlorotolueneHCID 7238—
반응물Lithium amideHCID 24532—
반응물2-(Di-tert-butylphosphino)biphenylHCID 2734215—
반응물Sodium t-butoxideHCID 23676156—
촉매(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
생성물Benzenamine, 2-methyl-N-(2-methylphenyl)-HCID 13642372%

반응 단계

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)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828986B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-6dc0c40063fa4ce2bed62a222591a84e
출처 메모uspto-grants-2014_09