반응 #307052

ord-98f3cacdfd4142f4b412f292328078fa

반응 방정식

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
수율 89.0%
CC1CCCCN1c1ccc(Br)cc1C=O
5-bromo-2-(2-methylpiperidin-1-yl)benzaldehyde
수율 89.0%

용매

반응 조건

온도
120°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도to cool to RT
  2. 2
    기타Reaction mixture
  3. 3
    기타was partitioned between H2O (1 L) and Et2O (2×750 mL)
  4. 4
    세척the combined organic layers were washed with brine (500 mL, pH 5-6 adjusted with HCl)
  5. 5
    건조dried over MgSO4
  6. 6
    여과filtered
  7. 7
    기타dried under vacuum

실험 절차

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%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08202865B2uspto-grants-2012_06