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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 254422생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/254422

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 2111338871.3%

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-butyl-lithium (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 160 g of the title product compound as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07875634B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-608618a1e2a1418e960fcf32652ae234
출처 메모uspto-grants-2011_01