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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 642259생성일: 2026년 10월 26일

Ethyl Acetoacetate → ethyl 2-methyl-1H-indole-3-carboxylate

https://huagongshe.com/reaction/642259

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetoacetateHCID 8868—
반응물2-IodoanilineHCID 11995—
반응물SodiumHCID 5360545—
용매AmmoniaHCID 222—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매tert-Butyl methyl etherHCID 15413—
생성물ethyl 2-methyl-1H-indole-3-carboxylateHCID 407235826.4%

반응 조건

온도120 °C

반응 단계

A mixture of 2-iodo-phenylamine (44.30 g, 202 mmol), sodium salt of ethyl acetoacetate (42.1 g, 263 mmol), and Cu(I)I (50.1 g, 263 mmol) in DMF (200 mL) was stirred at 120° C. overnight. Then the reaction mixture was cooled to room temperature, then diluted with methyl tert-butyl ether (MTBE) and water, and concentrated ammonia was added to dissolve the solid, the two layers were separated, the water layer was back extracted with MTBE; all MTBEs were combined and washed with sat. NaCl aqueous solution, dried over anhydrous sodium sulfate, filtered, and concentrated sequentially. The residue was crystallized in hexanes/EtOAc, giving the desired product (10.84 g), the mother liquor was concentrated and purified on column to give an additional batch of product (4.76 g). The title compound, 1H NMR (200 MHz, CDCl3): δ (ppm)=8.32 (1H), 8.09 (m, 1H), 7.31-7.13 (m, 3H), 4.39 (q, 2H, J=6.8 Hz), 2.74 (s, 3H), 1.45 (t, 3H, J=6.8 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07696223B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-afd5d3a8e9184f71b977a6b7f82c2303
출처 메모uspto-grants-2010_04