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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13997생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Potassium CarbonateHCID 11430—
반응물Carbamide PeroxideHCID 31294—
반응물3-Cyano-5-[(dipropylamino)carbonyl]Benzoic AcidHCID 22593638—
용매WaterHCID 962—
생성물3-Carbamoyl-5-dipropylcarbamoyl-benzoic acidHCID 22394891—

반응 조건

온도22.5 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727997B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-4776f860dc374479bbd3bed71c13955f
출처 메모uspto-grants-2010_06