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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1167988생성일: 2026년 10월 25일

Phenylboronic Acid → 3-Chloro-4-phenyl-1,2,5-thiadiazole

https://huagongshe.com/reaction/1167988

반응식

참여 물질

역할이름HCID투입량
반응물Phenylboronic AcidHCID 66827—
반응물Potassium FluorideHCID 522689—
반응물3-Bromo-4-chloro-1,2,5-thiadiazoleHCID 10125134—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
생성물3-Chloro-4-phenyl-1,2,5-thiadiazoleHCID 276404495%

반응 단계

To a mixture of 3-bromo-4-chloro-1,2,5-thiadiazole (0.2 g, 1 mmol), phenylboronic acid (0.135 g, 1.1 mol) in toluene (5 ml) is added a 1M aqueous solution of KF (3 cc, 3 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.055 g, 0.05 mmol, 5%mol) and the biphasic mixture is refluxed with vigorous stirring for 26 hours. The organic layer is decanted off and the aqueous layer is extracted with toluene (2×10 ml). After drying over magnesium sulfate and concentration under vacuum, the oily material is purified by flash chromatography on silica gel eluting with hexane/ethyl acetate (99/1) to afford 0.18 g (95%) of 3-chloro-4-phenyl-1,2,5-thiadiazole as a colorless oil, which crystallizes on standing (melting point 33° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06620940B1
출처 데이터셋uspto-grants-2003_09
ORD IDord-e2afbbc0167d4e4cb6251b72d214d0f3
출처 메모uspto-grants-2003_09