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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 892429생성일: 2026년 10월 25일

2-n-Octyl-4-isothiazolin-3-one → N-n-Octyl-cis-3-{[1-phenyl-3-(1-methylpyrrol-2-yl)-1,3-propanedionyl]thio}acrylamide

https://huagongshe.com/reaction/892429

반응식

참여 물질

역할이름HCID투입량
반응물2-n-Octyl-4-isothiazolin-3-oneHCID 33528—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물1-(1-Methylpyrrol-2-yl)-3-phenyl-1,3-propanedioneHCID 19895368—
용매Hydrochloric AcidHCID 313—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물N-n-Octyl-cis-3-{[1-phenyl-3-(1-methylpyrrol-2-yl)-1,3-propanedionyl]thio}acrylamideHCID 8674588119%

반응 단계

To a stirred solution of 0.78 g (0.0034 mol) of 1-(1-methylpyrrol-2-yl)-3-phenyl-1,3-propanedione in 5 mL of N,N-dimethylformamide under nitrogen was added 3.4 mL (0.0034 mol) of a 1M solution of tetrabutylammonium fluoride in tetrahydrofuran. After 10 min a solution of 0.73 g (0.0034 mol) of 2-n-octyl-4-isothiazolin-3-one in 5 mL of N,N-dimethylformamide was added. After 12 h another 3.4 mL of the 1M tetrabutylammonium fluoride solution was added. After 12 h the reaction mixture was diluted with 10% aqueous hydrochloric acid and extracted three times with ethyl acetate. The combined organic layers were washed several times with water, once with brine, and dried over magnesium sulfate. Removal of solvents and recrystallization of the crude product from ethyl acetate/hexane gave 0.28 g (19% yield) of N-n-Octyl-cis-3-{[1-phenyl-3-(1-methylpyrrol-2-yl)-1,3-propanedionyl]thio}acrylamide as a white solid, m.p. 131°-132° C. See Table 1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05118681
출처 데이터셋uspto-grants-1992_06
ORD IDord-5726f35de72e4be088d74d4981417cbc
출처 메모uspto-grants-1992_06