関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cfc 113 | HCID 6428 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 4-Methylcatechol | HCID 9958 | — |
| 反応物 | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| 反応物 | Pentamethyldiethylenetriamine | HCID 18196 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-chloro-5-fluoro-1H-indole-3-carboxylic acid | HCID 118644717 | 73.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09434724B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-62f0612a44624501baa69ff92d0919ac |
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| 出典メモ | uspto-grants-2016_09 |
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