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HRID 18629作成日:2026年10月24日

Aspirin → 4-Carbamoylphenyl 2-acetoxybenzoate

https://huagongshe.com/ja/reaction/18629

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4-HydroxybenzamideHCID 65052—
反応物HCID 178418300HCID 178418300—
溶媒ChloroformHCID 6212—
溶媒DimethylformamideHCID 6228—
生成物4-Carbamoylphenyl 2-acetoxybenzoateHCID 5934559247%

反応条件

温度0 °C

反応手順

To the solution of 1 (acetylsalicylic acid, 500 mg, 2.77 mmol) in 15 mL of dimethylformamide, hydroxybenzotriazole (412 mg, 3.05 mmol) and DCC (628 mg, 3.05 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 4-hydroxybenzamide (4, 418 mg, 3.05 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 chloroform; the organic layer was washed with brine, dried on anhydrous MgSO4, filtered and the solvent evaporated. The crude product 5 was loaded on a silica gel open column and eluted with CH2Cl2/MeOH (9/1), from which 4-carbamoylphenyl 2-acetoxybenzoate (5) was obtained (410 mg, 47% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741359B2
出典データセットuspto-grants-2010_06
ORD IDord-11293029832f43868d0ac3067b1a6d6f
出典メモuspto-grants-2010_06