反応 #307052

ord-98f3cacdfd4142f4b412f292328078fa

反応方程式

O=Cc1cc(Br)ccc1F
5-bromo-2-fluorobenzaldehyde
CC1CCCCN1
2-methylpiperidine
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CC1CCCCN1c1ccc(Br)cc1C=O
title compound
収率 89.0%
CC1CCCCN1c1ccc(Br)cc1C=O
5-bromo-2-(2-methylpiperidin-1-yl)benzaldehyde
収率 89.0%

溶媒

反応条件

温度
120°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度to cool to RT
  2. 2
    その他Reaction mixture
  3. 3
    その他was partitioned between H2O (1 L) and Et2O (2×750 mL)
  4. 4
    洗浄the combined organic layers were washed with brine (500 mL, pH 5-6 adjusted with HCl)
  5. 5
    乾燥dried over MgSO4
  6. 6
    ろ過filtered
  7. 7
    その他dried under vacuum

実験手順

To a solution of 5-bromo-2-fluorobenzaldehyde (13.20 g; 65.02 mmol) in DMSO (160 mL) and water (40 mL) were added 2-methylpiperidine (15.35 mL; 130.04 mmol) and anhydrous sodium carbonate (13.78 g; 130.04 mmol). The resulting mixture was heated at 120° C. for 16 h after which it was allowed to cool to RT. Reaction mixture was partitioned between H2O (1 L) and Et2O (2×750 mL) and the combined organic layers were washed with brine (500 mL, pH 5-6 adjusted with HCl), dried over MgSO4, filtered and dried under vacuum to give the title compound as a brown yellow oil (16.3 g, 89%). LC/MS (Method B): 282.1 (M+H)+. HPLC (Method A): Rt 2.20 min (Purity: 93.7%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08202865B2uspto-grants-2012_06