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HRID 44163作成日:2026年10月26日

Aspirin → 4-(3-Thioxo-3H-1,2-dithiol-5-yl)phenyl 2-acetoxybenzoate

https://huagongshe.com/reaction/44163

反応式

関与物質

役割名称HCID仕込み量
反応物AspirinHCID 2244—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物Desmethylanethol trithioneHCID 3082127—
反応物HCID 178418300HCID 178418300—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物4-(3-Thioxo-3H-1,2-dithiol-5-yl)phenyl 2-acetoxybenzoateHCID 1171803440%

反応条件

温度0 °C

反応手順

To the solution of 1 (acetylsalicylic acid, 416 mg, 2.31 mmol) in 40 mL of dimethylformamide, hydroxybenzotriazole (343 mg, 2.54 mmol) and DCC (523 mg, 2.54 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 5-p-hydroxyphenyl-1,2-dithiole-3-thione (2; 574 mg, 2.54 mmol) was added and stirred for 1 h at 0° C. and 3 h at room temperature. After filtration, the filtrate was evaporated under reduced pressure to remove the solvent. The oily residue thus obtained was dissolved in ethyl acetate; the organic layer was washed with brine, dried on anhydrous MgSO4, filtered and the solvent evaporated. The crude product was loaded on a silica gel open column and eluted with ethyl ether/petroleum ether (1/1), from which 4-(5-thioxo-5H-1,2-dithiol-3-yl)phenyl 2-acetoxybenzoate (3) was obtained (354 mg, 40% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541398B2
出典データセットuspto-grants-2013_09
ORD IDord-11d94d32732e42d884ebce9b705728f8
出典メモuspto-grants-2013_09