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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2284310생성일: 2026년 10월 27일

Benzenesulfonyl chloride → 1-benzenesulfonyl-3-bromo-6-nitro-1H-indole

https://huagongshe.com/reaction/2284310

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chlorideHCID 7369—
반응물Sodium hydrideHCID 24758—
반응물3-Bromo-6-nitro-1H-indoleHCID 14707934—
용매TetrahydrofuranHCID 8028—
생성물1-benzenesulfonyl-3-bromo-6-nitro-1H-indoleHCID 5744219676.5%

반응 단계

Sodium hydride (461 mg, 11.5 mmol) was slowly added to a solution of 3-bromo-6-nitro-1H-indole (2.32 g, 9.61 mmol) in tetrahydrofuran (10.0 mL). After stirring for 5 min, benzenesulfonyl chloride (1.47 mL, 11.5 mmol) was added dropwise over 10 min. The reaction was stirred an additional 1.5 h before quenching with 5.0 mL of methanol, followed by 10.0 mL water and 20.0 mL methylene chloride. The precipitate was filtered off and washed with an excess of methylene chloride and methanol to give a crème-colored powder for 3-bromo-6-nitro-1-(phenylsulfonyl)-1H-indole (2.80 g, 7.35 mmol, 76%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09144557B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-61e947e1665143c7be2c4f5506605dfa
출처 메모uspto-grants-2015_09