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Sodium Hydroxide → 4-(Benzyloxy)-2-[(heptylsulfinyl)methyl]-3-methylquinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | m-Chloroperbenzoic acid | HCID 70297 | — |
| 反応物 | 4-(Benzyloxy)-2-[(heptylsulfanyl)methyl]-3-methylquinoline | HCID 59527296 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-(Benzyloxy)-2-[(heptylsulfinyl)methyl]-3-methylquinoline | HCID 59527314 | 68% |
反応手順
To a solution of 4-(benzyloxy)-2-[(heptylsulfanyl)methyl]-3-methylquinoline (106 mg) in dichloromethane (5 mL) was added m-chloroperbenzoic acid (75%, 68 mg) at −30° C., followed by stirring for 5 hours while warming to room temperature. A 0.2M aqueous sodium hydroxide solution (20 mL) was added to the reaction mixture, followed by extraction with chloroform (50 mL). The organic layer was washed sequentially with water and saturated brine and then dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: chloroform/methanol=10/1) to obtain 4-(benzyloxy)-2-[(heptylsulfinyl)methyl]-3-methylquinoline (75 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08367702B2 |
| 出典データセット | uspto-grants-2013_02 |
| ORD ID | ord-d58d66f255d94c5cbadca1ba63e3abc4 |
| 出典メモ | uspto-grants-2013_02 |