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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 515958생성일: 2026년 10월 27일

Dicyclohexylcarbodiimide → Ethyl 4-(1,3-dioxoisoindolin-2-YL)-3-oxobutanoate

https://huagongshe.com/reaction/515958

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
반응물N-PhthaloylglycineHCID 20825—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물Ethyl 4-(1,3-dioxoisoindolin-2-YL)-3-oxobutanoateHCID 70123985%

반응 단계

To a solution of 2-(1,3-dioxoisoindolin-2-yl)acetic acid (3.01 g, 14.67 mmol), 2,2-dimethyl-1,3-dioxane-4,6-dione (2.23 g, 15.47 mmol) and 4-dimethylaminopyridine (2.73 g, 22.35 mmol) in dichloromethane (150 mL) was added a solution of DCC (3.36 g, 16.28 mmol) in DCM (50 mL) at 0° C. The mixture was stirred at RT for 16 h. The insoluble materials were filtered off, and the filtrate was washed with 5% NaHSO4 aqueous solution. The organic phase was dried over anhydrous Na2SO4, filtered and the filtrate was concentrated under reduced pressure. The residue was treated with EtOH (200 mL) and the resulting mixture was stirred at 70° C. for 4 h and then concentrated under reduced pressure. Water was added to the residue and the mixture was extracted with EtOAc. The organic layers were washed with water and brine, dried over anhydrous MgSO4, and filtered. The filtrate was concentrated under reduced pressure and the residue was washed with IPE to give the title compound as a colorless solid (3.43 g, 85%). 1H NMR (400 MHz, CDCl3) δ ppm 1.31 (t, J=6.8 Hz, 3H), 3.58 (s, 2H), 4.24 (q, J=6.8 Hz, 2H), 4.67 (s, 2H), 7.73-7.78 (m, 2H), 7.86-7.91 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09108970B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-e9dc617c7bfb493681438194a1883e98
출처 메모uspto-grants-2015_08