戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 13997作成日:2026年10月24日

Acetone → 3-Carbamoyl-5-dipropylcarbamoyl-benzoic acid

https://huagongshe.com/ja/reaction/13997

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Potassium CarbonateHCID 11430—
反応物Carbamide PeroxideHCID 31294—
反応物3-Cyano-5-[(dipropylamino)carbonyl]Benzoic AcidHCID 22593638—
溶媒WaterHCID 962—
生成物3-Carbamoyl-5-dipropylcarbamoyl-benzoic acidHCID 22394891—

反応条件

温度22.5 °C

反応手順

A mixture of 3-cyano-5-[(dipropylamino)carbonyl]benzoic acid (IX/XXXII, PREPARATION 7, 0.602 g, 2.19 mmol), potassium carbonate (0.212 g, 1.53 mmol), and acetone (2.5 mL) is stirred at 20-25 degrees C. Water (2.5 mL) and urea-hydrogen peroxide adduct (0.825 g, 8.78 mmol) are added and the mixture is stirred for 15 hours at 20-25 degrees C., at which time additional urea-hydrogen peroxide adduct (0.204 g) is added; after stirring for another 3 hours, an additional 0.205 g of urea-hydrogen peroxide is added. After a total of 39 hours has elapsed, the acetone is removed under reduced pressure and the residue is acidified with hydrochloric acid (3N) to pH=2-4. The mixture is extracted with dichloromethane, the organic layer is separated and washed with hydrochloric acid (0.5 N), and the organic phase is dried with anhydrous magnesium sulfate to a solid. The solid is crystallized from dichloromethane/hexane/methanol to give the title compound, MS (ESI+) for C15H20N2O4 m/z (M+H)+=293.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727997B2
出典データセットuspto-grants-2010_06
ORD IDord-4776f860dc374479bbd3bed71c13955f
出典メモuspto-grants-2010_06