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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 268761생성일: 2026년 10월 25일

Aniline → Phenyl-(1-triisopropylsilanyl-1H-indol-4-yl)-amine

https://huagongshe.com/reaction/268761

반응식

참여 물질

역할이름HCID투입량
반응물AnilineHCID 6115—
반응물Potassium CarbonateHCID 11430—
반응물4-bromo-1-(triisopropylsilyl)-1H-indoleHCID 2795573—
용매tert-ButanolHCID 6386—
생성물Phenyl-(1-triisopropylsilanyl-1H-indol-4-yl)-amineHCID 59831613—

반응 조건

온도110 °C

반응 단계

Aniline (328 μl, 3.6 mmol) was added to a room temperature mixture of 4-bromo-1-triisopropylsilanyl-1H-indole (1.06 g, 3 mmol), tris(dibenzylideneacetone)dipalladium 2-(dicyclohexylphosphino)-2,4,6-triisopropyl-1,1′-biphenylphosphine (Pd2(dba)3, 27.5 mg, 0.03 mmol), (72 mg, 0.05 mmol) and K2CO3 (1.04 g, 7.5 mmol) in t-BuOH (14 ml). The reaction mixture was stirred at 110° C. for 4 hours. The reaction was cooled, and the solid was filtered off. The filtrate was concentrated and the residue was partitioned between EtOAc and a saturated solution of NaHCO3. The aqueous layer was extracted twice with EtOAc. The combined organic layers were dried over Na2SO4, filtered, concentrated, and purified via flash chromatography (hexane/EtOAc) affording the compound XXI as a yellow oil in quantitative yield (1.09 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07446118B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-6ffbe1855af64e399956cba235bb565e
출처 메모uspto-grants-2008_11