참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cfc 113 | HCID 6428 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 4-Methylcatechol | HCID 9958 | — |
| 반응물 | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| 반응물 | Pentamethyldiethylenetriamine | HCID 18196 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-chloro-5-fluoro-1H-indole-3-carboxylic acid | HCID 118644717 | 73.8% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434724B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-62f0612a44624501baa69ff92d0919ac |
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| 출처 메모 | uspto-grants-2016_09 |
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