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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8633생성일: 2026년 10월 23일

Dichloromethane → 2,5-Dichloro-4-methylthiophene-3-sulfonyl chloride

https://huagongshe.com/ko/reaction/8633

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물3-MethylthiopheneHCID 12024—
반응물Chlorosulfonic acidHCID 24638—
반응물Sulfuryl chlorideHCID 24648—
생성물2,5-Dichloro-4-methylthiophene-3-sulfonyl chlorideHCID 2198379625%

반응 조건

온도10 °C

반응 단계

To a cooled (10° C.) solution of 3-methylthiophene (5 g, 50 mmol) in dichloromethane (15 mL) was added a solution of sulfuryl chloride (8.6 mL) in dichloromethane (5 mL). The reaction mixture was maintained at 10° C. for 30 minutes, then at ambient temperature for 16 hours. The reaction was concentrated and redissolved in dichloromethane (30 mL) and cooled to −10° C. To the cooled solution was added chlorosulfonic acid (2 mL, 100 mmol). The reaction was maintained at −10° C. for 30 minutes, then at ambient temperature for 16 hours, at which time it was poured into ice water (50 mL) and extracted with dichloromethane (50 mL). The organic layer was dried (Mg2SO4) and concentrated to furnish a brown oil (3.3 g, 25%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091204B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-d3a94c6cd2a949a99cb74eb9ff971a3b
출처 메모uspto-grants-2006_08