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HRID 57321作成日:2026年10月23日

Cfc 113 → 4-chloro-5-fluoro-1H-indole-3-carboxylic acid

https://huagongshe.com/ja/reaction/57321

反応式

関与物質

役割名称HCID仕込み量
反応物Cfc 113HCID 6428—
反応物TetrahydrofuranHCID 8028—
反応物4-MethylcatecholHCID 9958—
反応物2,2,6,6-TetramethylpiperidineHCID 13035—
反応物PentamethyldiethylenetriamineHCID 18196—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
生成物4-chloro-5-fluoro-1H-indole-3-carboxylic acidHCID 11864471773.8%

反応条件

温度-78 °C

反応手順

2,2,6,6-Tetramethylpiperidine (1.06 g, 7.5 mmol), N,N′,N″,N″-pentamethyldiethylene triamine (3.46 g, 20 mmol) and compound 1 (1.45 g, 5.0 mmol) were added consecutively to a solution of n-BuLi (2.5 M in hexanes, 8 mL, 20 mmol) in THF (20 mL) and hexanes (6 mL) at −78° C. After stirring for 4 h at −78° C., the mixture was treated with 1,1,2-trichloro-1,2,2-trifluoroethane (1.18 g, 6.0 mmol) before it was warmed to 25° C. Water was added to the mixture. The organic phase was washed with brine, dried with sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by SiO2 column chromatography (PE) to provide title compound (1.2 g, 73.8%) as a colorless liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434724B2
出典データセットuspto-grants-2016_09
ORD IDord-62f0612a44624501baa69ff92d0919ac
出典メモuspto-grants-2016_09