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Sodium borohydride → (5-Bromo-2-(2-methylpiperidin-1-YL)phenyl)methanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 5-Bromo-2-(2-methylpiperidin-1-YL)benzaldehyde | HCID 23091101 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Ammonium Chloride | HCID 25517 | — |
| 生成物 | (5-Bromo-2-(2-methylpiperidin-1-YL)phenyl)methanol | HCID 58554197 | 97% |
反応手順
To a solution of 5-bromo-2-(2-methylpiperidin-1-yl)benzaldehyde (16.30 g; 57.76 mmol) in MeOH (300 mL) was added sodium borohydride (2.19 g; 57.76 mmol) at 5° C. in a portion-wise fashion and stirred for 30 min. After this time, reaction mixture was diluted with a saturated aqueous solution of NH4Cl (300 mL), extracted with EtOAc. The org layers were washed with aqueous solution of NH4Cl (150 mL), brine (300 mL), dried over MgSO4 and evaporated under vacuum to give the title compound as a yellow oil (15.9 g, 97%). LC/MS (Method A): 285.6 (M+H)+. HPLC (Method A): Rt 2.13 min (Purity: 94.9%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08202865B2 |
| 出典データセット | uspto-grants-2012_06 |
| ORD ID | ord-7623db50dd62442a9174e143c5e24cd4 |
| 出典メモ | uspto-grants-2012_06 |