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HRID 892429作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物2-n-Octyl-4-isothiazolin-3-oneHCID 33528—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物1-(1-Methylpyrrol-2-yl)-3-phenyl-1,3-propanedioneHCID 19895368—
溶媒Hydrochloric AcidHCID 313—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物N-n-Octyl-cis-3-{[1-phenyl-3-(1-methylpyrrol-2-yl)-1,3-propanedionyl]thio}acrylamideHCID 8674588119%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05118681
出典データセットuspto-grants-1992_06
ORD IDord-5726f35de72e4be088d74d4981417cbc
出典メモuspto-grants-1992_06