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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61938생성일: 2026년 10월 26일

Hexachloroethane → 3-Chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamide

https://huagongshe.com/reaction/61938

반응식

참여 물질

역할이름HCID투입량
반응물HexachloroethaneHCID 6214—
반응물N,N-dimethyl-1H-pyrazole-1-sulfonamideHCID 10954038—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물3-Chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamideHCID 21113388—

반응 조건

온도-78 °C

반응 단계

To a solution of N-dimethylsulfamoylpyrazole (188.0 g, 1.07 mol) in dry tetrahydrofuran (1500 mL) at −78° C. was added dropwise a solution of 2.5 M n-butyllithium (472 mL, 1.18 mol) in hexane while maintaining the temperature below 65° C. Upon completion of the addition the reaction mixture was maintained at −78° C. for an additional 45 minutes, after which time a solution of hexachloroethane (279 g, 1.18 mol) in tetrahydrofuran (120 mL) was added dropwise. The reaction mixture was maintained for an hour at −78° C., warmed to −20° C. and then quenched with water (1 L). The reaction mixture was extracted with methylene chloride (4×500 mL); the organic extracts were dried over magnesium sulfate and concentrated. The crude product was further purified by chromatography on silica gel using methylene chloride as eluent to afford the title product compound as a yellow oil (160 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09445593B1
출처 데이터셋uspto-grants-2016_09
ORD IDord-8f699849a5c84fca8d42d8812131cebc
출처 메모uspto-grants-2016_09