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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 888259생성일: 2026년 10월 25일

Hexane → 2-[2-(Benzenesulfonyl)-ethylsulfanyl]-3-nitropyridine

https://huagongshe.com/reaction/888259

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물2-Chloro-3-nitropyridineHCID 79613—
반응물2-(Phenylsulfonyl)ethanethiolHCID 447093—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물2-[2-(Benzenesulfonyl)-ethylsulfanyl]-3-nitropyridineHCID 6713375746%

반응 단계

1.8 g (16.0 mmol) potassium tert-butylate were added to a solution of 3.0 g (14.8 mmol) 2-(phenylsulfonyl)ethanethiol in DMF (35 ml) and the mixture was stirred for 30 min at room temperature. Then 2.5 g (15.8 mmol) 2-chloro-3-nitropyridine were added and the mixture was stirred for a further 1 h at RT. Then it was diluted with a brine/EE mixture (1:1 vv) and stirred for a further 30 min at RT. Then the organic phase was separated off, washed with water and brine, dried over Na2SO4, filtered and concentrated to small volume under vacuum. Column chromatography (hexane/EE 6:1) of the residue yielded 2.2 g (6.8 mmol, 46%) 2-[2-(benzenesulfonyl)-ethylsulfanyl]-3-nitropyridine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08247573B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-6cd212b40b0f4f10b0d04144f712bace
출처 메모uspto-grants-2012_08