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HRID 642259作成日:2026年10月27日

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

https://huagongshe.com/reaction/642259

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetoacetateHCID 8868—
反応物2-IodoanilineHCID 11995—
反応物SodiumHCID 5360545—
溶媒AmmoniaHCID 222—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒tert-Butyl methyl etherHCID 15413—
生成物ethyl 2-methyl-1H-indole-3-carboxylateHCID 407235826.4%

反応条件

温度120 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07696223B2
出典データセットuspto-grants-2010_04
ORD IDord-afd5d3a8e9184f71b977a6b7f82c2303
出典メモuspto-grants-2010_04