関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetaldehyde | HCID 177 | — |
| 反応物 | 1,3-Difluoro-5-iodobenzene | HCID 2778221 | — |
| 反応物 | 1,2,2,3-Tetramethylpiperidine | HCID 18761772 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-(2,6-Difluoro-4-iodophenyl)ethanol | HCID 67001299 | 47.4% |
反応手順
To a solution of 2.5 M n-butyl lithium in hexanes (2 mL, 5.0 mmol) and tetrahydrofuran (20 mL) at −78° C. under an atmosphere of nitrogen was added dropwise tetramethylpiperidine (0.85 mL, 5.0 mmol). The resulting light yellow solution was stirred for approximately 15 minutes, then 1,3-difluoro-5-iodo-benzene (1 g, 4.17 mmol) was added dropwise. This solution was stirred at −78° C. for 1 hour, followed by the addition of acetaldehyde (0.70 mL, 12.5 mmol) via syringe. The reaction mixture was stirred at −78° C. for 10 minutes then allowed to warm to room temperature. TLC indicated the reaction to be complete. The reaction was quenched with saturated aqueous ammonium chloride solution (2 mL), diluted with water (50 mL) and extracted with ethyl acetate (2×30 mL). The combined organic layers were dried over sodium sulfate and concentrated in vacuo. The crude product was purified by chromatography over silica gel gradient eluted with 0 to 25% v/v ethyl acetate/hexanes to give 1-(2,6-difluoro-4-iodo-phenyl)-ethanol (561 mg, 47%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08063085B2 |
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| 出典データセット | uspto-grants-2011_11 |
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| ORD ID | ord-4732835dd49a442cbe2e7f06b3806d3e |
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| 出典メモ | uspto-grants-2011_11 |
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