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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 344710생성일: 2026년 10월 25일

Acetic Acid → 5-Chloro-2-(methylsulfonyl)benzo[d]thiazole

https://huagongshe.com/reaction/344710

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrogen PeroxideHCID 784—
반응물Sodium ThiosulfateHCID 24477—
반응물Potassium PermanganateHCID 516875—
반응물5-Chloro-2-(methylthio)benzothiazoleHCID 645746—
생성물5-Chloro-2-(methylsulfonyl)benzo[d]thiazoleHCID 21985716100%

반응 단계

A mixture of 1.80 g (8.34 mmols) of 5-chloro-2-methylthiobenzothiazole, 1.80 g (11.39 mmols) of potassium permanganate and 45 ml of 50% aqueous acetic acid solution was stirred at room temperature for an hour. After the reaction, a 30.0 to 35.5% aqueous hydrogen peroxide solution was dropwise added to the mixture with stirring under ice cooling until to be colorless. An aqueous sodium thiosulfate was added to the mixture followed by extraction of the solution with chloroform. The chloroform layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to afford 2.05 g (yield: 100%) of 5-chloro-2-methanesulfonylbenzothiazole. A mixture of 1.64 g (6.62 mmols) of the above compound, 2.57 g (9.91 mmols) of Compound b obtained in Reference Example 2 and 40 ml of acetonitrile was heated under reflux for 20 hours. The mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: chloroform/methanol =100/1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05053408
출처 데이터셋uspto-grants-1991_10
ORD IDord-e85f73c011aa41a6a1003f561526603f
출처 메모uspto-grants-1991_10