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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1751100생성일: 2026년 10월 24일

Acetic Acid → Methyl 3-(2-oxoindolin-3-yl)propanoate

https://huagongshe.com/ko/reaction/1751100

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrochloric AcidHCID 313—
반응물Dimethyl SulfoxideHCID 679—
반응물Methyl 3-(1H-indol-3-yl)propanoateHCID 21711—
용매WaterHCID 962—
생성물Methyl 3-(2-oxoindolin-3-yl)propanoateHCID 1490358398%

반응 단계

A mixture of methyl 3-indolepropionate (5.00 g, 0.0246 mol), acetic acid (10 mL), dimethylsulfoxide (26 mL, 0.369 mol, 15 eq.) and concentrated hydrogen chloride (37%) (22 mL, 0.738 mol, 30 eq.) was stirred at ambient temperature for 2.5 h. Water was added to the mixture and the mixture was extracted with ethyl acetate. The organic layer was dried over MgSO4, filtered and concentrated in vacuo. The crude residue was purified using the Biotage flash chromatography system (30% ethyl acetate in hexanes) to afford the title compound as an oil (5.28 g, 98%); 1H NMR (DMSO-d6); 62.03-2.10 (m, 2H); 2.32-2.39 (m, 2H); 3.46 (t, J=6.4 Hz, 1H); 3.54 (s, 3H); 6.81 (d, J=7.6 Hz, 1H); 6.93-6.97 (m, 1H); 7.15-7.17 (m, 1H); 7.24 (d, J=7.6 Hz, 1H);

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09156840B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-56aedeab4e41445cabcf3cd9901bb1a6
출처 메모uspto-grants-2015_10