関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 4-Methanesulfonylpyridine | HCID 292487 | — |
| 反応物 | HCID 15790522 | HCID 15790522 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | HCID 15790523 | HCID 15790523 | — |
反応手順
To a suspension of 0.2 g of 60% NaH (as an oil dispersion, 0.005 m) in 5 mL of DMF was added 1.41 g (0.005 m) of 2-[4-[4-(trifluoromethyl)phenoxy]phenyl]ethanol. The mixture was stirred at room temperature for 30 minutes, until hydrogen evolution ceased. To the mixture was then added 0.79 g (0.005 m) of 4-(methylsulfonyl)pyridine, and the mixture was stirred overnight am room temperature. Excess DMF was then removed in vacuo. The resulting material was diluted with water, and the product was extracted into CH2Cl2. The CH2Cl2 layer was separated and filtered through phase separating paper, then concentrated. The residue was adsorbed onto silica gel and chromatographed, eluting with CH2Cl2 →30% EtOAc/CH2Cl2. The resulting material was rechromatographed over fine-particle silica gel, eluting with CH2Cl2 →50% EtOAc/CH2Cl2. Yield 0.5 g.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05597836 |
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| 出典データセット | uspto-grants-1997_01 |
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| ORD ID | ord-2d2b9369f62147bd9152c60190b2ffeb |
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| 出典メモ | uspto-grants-1997_01 |
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