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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1532456생성일: 2026년 10월 26일

Triethylamine → 5-[2-(Phenylsulfonyl)ethenyl]indole

https://huagongshe.com/reaction/1532456

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물5-BromoindoleHCID 24905—
반응물2-(Phenylsulfonyl)ethanolHCID 30202—
반응물Tri-o-tolylphosphineHCID 80271—
반응물Methanesulfonic anhydrideHCID 81560—
촉매palladium(II) acetateHCID 167845—
용매AcetonitrileHCID 6342—
생성물5-[2-(Phenylsulfonyl)ethenyl]indoleHCID 5432856023.3%

반응 조건

온도50 °C

반응 단계

To 0.186 g (1.0 mmol) of 2-(phenylsulfonyl)ethanol, 3 ml of acetonitrile was added, followed by 0.19 g(1.1 mmol) of methanesulfonic anhydride and 0.56 ml (4.0 mmol) of triethylamine, and the mixture was stirred for 5 hours at an internal temperature of 50° C. Subsequently, 0.29 g (1.5 mmol) of 5-bromoindole, 0.011 g (0.05 mmol) of palladium acetate, and 0.067 g (0.22 mmol) of tri(o-tolyl)phosphine were added, and the mixture was then refluxed for 17 hours. After cooled to room temperature, the reaction mixture was concentrated and purified by column chromatography (hexane/ethyl acetate=70/30) to obtain 0.066 g of 5-[2-(phenylsulfonyl)ethenyl]indole. Yield: 23%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06201131B1
출처 데이터셋uspto-grants-2001_03
ORD IDord-90fb7022e82a4cb485d643bf37510e97
출처 메모uspto-grants-2001_03