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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1781615생성일: 2026년 10월 26일

Chlorine → 1,2-Benzisothiazol-3(2H)-one

https://huagongshe.com/reaction/1781615

반응식

참여 물질

역할이름HCID투입량
반응물ChlorineHCID 24526—
반응물Sulfuryl chlorideHCID 24648—
반응물2-(Methylthio)benzaldehyde oximeHCID 786757—
용매ChlorobenzeneHCID 7964—
생성물1,2-Benzisothiazol-3(2H)-oneHCID 1752091.1%

반응 단계

From the monochlorobenzene layer obtained by the same procedures as in Example 1, 2-(methylthio)benzaldehyde oxime was isolated in the same manner as in Example 2. 39.7 g of the oxime isolated was dissolved in 150 g of monochlorobenzene. Then, the oxime was cyclized in the same manner as in Example 1 except that chlorine was changed to 35.3 g (0.26 mol) of sulfuryl chloride. As a result, 32.7 g of 1,2-benzisothiazol-3-one was obtained. The yield against 2-(methylthio)benzaldehyde oxime was 91%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05633384
출처 데이터셋uspto-grants-1997_05
ORD IDord-8e36c12d6bee48f7b869e675e19ea709
출처 메모uspto-grants-1997_05