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Ethanol → 2-(4-(1-Hydroxyethyl)phenyl)-5-decyloxypyrimidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Chloroform | HCID 6212 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 2-(4-Acetylphenyl)-5-decyloxypyrimidine | HCID 19694901 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-(4-(1-Hydroxyethyl)phenyl)-5-decyloxypyrimidine | HCID 21468280 | 99.9% |
反応手順
To a mixed solvent of 200 ml of ethanol and 100 ml of chloroform were added 35.5 g (0.1 mole) of 2-(4-acetylphenyl)-5-decyloxypyrimidine, and while maintaining the temperature at 30° to 35° C., 2.65 g (0.07 mole) of sodium borohydride were gradually added thereto. After stirring at the same temperature for 4 hours, the reaction mixture was poured into 500 ml of water and extracted with 400 ml of ethyl acetate. The organic phase was washed sufficiently, dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure to obtain 35.6 g (yield: 99.9 %) of 2-{4-(1-hydroxyethyl)phenyl}-5-decyloxypyrimidine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05693251 |
| 出典データセット | uspto-grants-1997_12 |
| ORD ID | ord-c9046b081e0f4cf0b15ce782fba6c387 |
| 出典メモ | uspto-grants-1997_12 |