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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 404305생성일: 2026년 10월 24일

4-Vinylbenzoic acid → 4-Vinylbenzoyl chloride

https://huagongshe.com/ko/reaction/404305

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참여 물질

역할이름HCID투입량
반응물4-Vinylbenzoic acidHCID 14098—
반응물Thionyl ChlorideHCID 24386—
촉매DimethylformamideHCID 6228—
용매TolueneHCID 1140—
생성물4-Vinylbenzoyl chlorideHCID 1105202870%

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온도60 °C

반응 단계

While 16.6 g of p-vinylbenzoic acid (manufactured by Wako Pure Chemical Industries, Ltd.), 80 ml of toluene, two drops of N,N-dimethylformamide were stirred at room temperature, 9.7 ml of thionyl chloride (manufactured by Wako Pure Chemical Industries, Ltd.) was added thereto, which was heated and stirred at 60° C. for 2 hours. The inside of the reaction system was cooled to 40° C., toluene and an excessive amount of thionyl chloride were removed under reduced pressure, and p-vinyl benzoic acid chloride was obtained. While 22.5 g of 2-aminoanthraquinone (manufactured by Tokyo Chemical Industry Co., Ltd.) and 110 ml of pyridine were stirred on ice, p-vinyl benzoic acid chloride was slowly added dropwise thereto. After stirring the mixture on ice for 30 minutes, the temperature was increased to 60° C. and the mixture was heat while stirring for 3 hours. Thereafter, the mixture was cooled to room temperature and water was added thereto. The resulting coarse crystals were filtrated and washed with water and methanol, and then 500 ml of methanol was added to the collected coarse crystals, and then heated while stirring at 60° C. Thereafter, the resultant crystals were separated by filtration, washed with methanol and dried. Thus, 20.1 g of M-19 was obtained (yield: 70%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748529B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-11504d18f3af4c2d931f0c94da90fd80
출처 메모uspto-grants-2014_06