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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239215생성일: 2026년 10월 26일

Water → 2-(3,4-Dichlorophenyl)-3-hydroxy-4-(methylcarbonyl)thiophene

https://huagongshe.com/reaction/239215

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물ChloroformHCID 6212—
반응물Sulfuryl chlorideHCID 24648—
반응물2-(3,4-Dichlorophenyl)-3-hydroxy-4-methylcarbonyl-2,5-dichlorothiopheneHCID 67159771—
용매IsopropanolHCID 3776—
생성물2-(3,4-Dichlorophenyl)-3-hydroxy-4-(methylcarbonyl)thiopheneHCID 4420728877.8%

반응 조건

온도-20 °C

반응 단계

A chloroform (967 mL) solution of 2-(3,4-dichlorophenyl)-3-hydroxy-4-methylcarbonyl-2,5-dichlorothiophene (96.7 g, 221 mmol, purity: 63%) was cooled to −18° C., and to this solution, a chloroform (193 mL) solution of sulfuryl chloride (19.5 mL, 1.15 equivalent amounts) was dropwise added over a period of 20 minutes, followed by stirring at −20° C. for 1 hour. The temperature of the solution was raised to 0° C., and water (193 mL) was dropwise added over a period of 5 minutes, followed by liquid separation. The obtained chloroform solution was sequentially washed with water, a saturated salt solution, a saturated sodium hydrogencarbonate aqueous solution, a saturated sodium thiosulfate aqueous solution and a saturated salt solution, and dried over anhydrous magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off to obtain a crude product. To the obtained crude product, 2-propanol (967 mL) was added, followed by stirring at 5° C. for 1 hour. The formed crystals were subjected to filtration to give the desired product as a pale yellow solid (49.4 g, yield: 51%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642786B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-fffe37e1d30e4993915eeef48515b46c
출처 메모uspto-grants-2014_02