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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 236233생성일: 2026년 10월 24일

2-Methylbenzothiazole → 2-Methylbenzo[d]thiazole-4-sulfonyl chloride

https://huagongshe.com/ko/reaction/236233

반응식

참여 물질

역할이름HCID투입량
반응물2-MethylbenzothiazoleHCID 8446—
반응물Chlorosulfonic acidHCID 24638—
생성물2-Methylbenzo[d]thiazole-4-sulfonyl chlorideHCID 13824425—

반응 단계

2-Methylbenzothiazole (50 g) was added in a slow, dropwise manner to 86 mL of chlorosulfonic acid at room temperature. When the addition was complete, the dark reaction mixture was heated at 140°-145° C. for about 3 hours. The solution was allowed to cool and was slowly added to a large excess of ice. Insoluble solids were removed by filtration and the aqueous layer was extracted with benzene. Drying and evaporation of the solvent gave an off-white solid which was shown by 1H NMR analysis to consist of a mixture of sulfonyl chlorides, presumably the 4-, 6-, and 7-isomers. This crude material was recrystallized three times from hexane to remove the 6-isomer as a white solid, m.p. 100°-102° C. The combined mother liquors were concentrated to give a dark yellow oil which was carried on to the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04643759
출처 데이터셋uspto-grants-1987_02
ORD IDord-3fe9f9e2bb2d48fa8c1ec81089209487
출처 메모uspto-grants-1987_02