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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252683생성일: 2026년 10월 26일

2-Bromo-4,6-dimethylaniline → N-(2-Bromo-4,6-dimethylphenyl)(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl) dimethylsilanamine

https://huagongshe.com/reaction/252683

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-4,6-dimethylanilineHCID 170579—
반응물Chloro(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl)dimethylsilaneHCID 58526148—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물N-(2-Bromo-4,6-dimethylphenyl)(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl) dimethylsilanamineHCID 58526146—

반응 단계

Under and argon atmosphere, to a solution of 14.8 g (74.2 mmol) of 2-bromo-4,6-dimethylaniline in 200 ml of THF, 29.7 ml of 2.5 M (74.2 mmol) nBuLi in hexanes was added at −80° C. This mixture was warmed for ca. 1 hour to ambient temperature. Then, the resulting solution was added dropwise for ca. 1 hour while vigorously stirring to a solution of 18.0 g (74.2 mmol) of chloro(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl)dimethylsilane in 100 ml of THF. The resulting mixture was stirred overnight at ambient temperature, then, evaporated to dryness. To the residue, 150 ml of toluene was added. This mixture was filtered through a glass frit (G4). The filtrate was evaporated to dryness. Fractional distillation gave a yellow liquid, bp 168-172° C./0.2 mm Hg. The product crystallizes slowly at ambient temperature. Yield 16.5 g (55%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07868197B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-35f68668ca2847aa9ae27e4f86ce4f4e
출처 메모uspto-grants-2011_01