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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1426654생성일: 2026년 10월 27일

Benzenesulfonyl chloride → 5-Bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde

https://huagongshe.com/reaction/1426654

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chlorideHCID 7369—
반응물Sodium hydrideHCID 24758—
반응물5-bromo-1H-pyrrole-3-carbaldehydeHCID 57831983—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물5-Bromo-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehydeHCID 8623280585.5%

반응 단계

To a solution of 5-bromo-1H-pyrrole-3-carbaldehyde (3.50 g) in tetrahydrofuran (70 mL) was added sodium hydride (60% in oil, 1.21 g) at room temperature, and the mixture was stirred for 10 min. Benzenesulfonyl chloride (4.27 g) was added, and the mixture was further stirred for 1 hr, diluted with water, and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=4:1→7:3) and crystallized from diisopropyl ether to give the title compound as colorless crystals (yield 5.4 g, 85%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08933105B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-65dd15020501426ebe740c5be79d578a
출처 메모uspto-grants-2015_01