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Hydrochloric Acid → 4-{[(2S)-2-fluoropropyl]oxy}pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Cyanomethylenetributylphosphorane | HCID 4622928 | — |
| 反応物 | (2S)-2-fluoropropan-1-ol | HCID 11528331 | — |
| 反応物 | HCID 178418642 | HCID 178418642 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 4-{[(2S)-2-fluoropropyl]oxy}pyridine | HCID 66696113 | 89.9% |
反応手順
A solution of 1.5 g of 4-hydroxypyridine, 7.6 g of cyanomethylenetributylphosphorane, and 1.4 g of (2S)-2-fluoro-1-propanol in 20 mL of toluene was stirred at 105° C. overnight. To the reaction mixture were added 1 M hydrochloric acid and ethyl acetate, and the organic layer was separated. The aqueous layer was adjusted to pH 11 by the addition of a 1 M aqueous sodium hydroxide solution, and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform/methanol) to obtain 2.2 g of 4-{[(2S)-2-fluoropropyl]oxy}pyridine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08822448B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-7a62bb2315da4ddd9ab4f2c528883a6b |
| 出典メモ | uspto-grants-2014_09 |