戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 219871作成日:2026年10月24日

Sodium borohydride → (5-Bromo-2-(2-methylpiperidin-1-YL)phenyl)methanol

https://huagongshe.com/ja/reaction/219871

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物5-Bromo-2-(2-methylpiperidin-1-YL)benzaldehydeHCID 23091101—
溶媒MethanolHCID 887—
溶媒Ammonium ChlorideHCID 25517—
生成物(5-Bromo-2-(2-methylpiperidin-1-YL)phenyl)methanolHCID 5855419797%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202865B2
出典データセットuspto-grants-2012_06
ORD IDord-7623db50dd62442a9174e143c5e24cd4
出典メモuspto-grants-2012_06