Iodoethane → 3-Chloro-2-ethoxybenzaldehyde

HRID 1362042

Reaktionsgleichung

Reaktionsgleichung von HRID 1362042
I[CH2:2][CH3:3].[Cl:4][C:5]1[C:6]([OH:13])=[C:7]([CH:10]=[CH:11][CH:12]=1)[CH:8]=[O:9].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[Cl:4][C:5]1[C:6]([O:13][CH2:2][CH3:3])=[C:7]([CH:10]=[CH:11][CH:12]=1)[CH:8]=[O:9]

Komponenten

5

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

Iodoethane (1.54 mL, 19.2 mmol) was added to a stirring solution of 3-chloro-2-hydroxy-benzaldehyde (2.01 g, 12.8 mmol) and K2CO3 (3.90 g, 28.2 mmol) in DMF (25 mL). The mixture was heated to 50° C. and stirred for 2.5 h. The heat was removed and reaction stirred at room temperature for 18 h. The reaction was quenched with H2O (70 mL). The mixture was extracted with EtOAc (3×50 mL). The combined organics were washed with brine (2×50 mL), dried over Na2SO4, filtered and concentrated to yield the title compound (2.16 g, 91%) as a yellow oil: 1H NMR (300 MHz, DMSO-d6) δ 10.27 (s, 1H), 7.85 (dd, J=7.8, 1.5 Hz, 1H), 7.72 (dd, J=7.8, 1.8 Hz, 1H), 7.33 (t, J=7.8 Hz, 1H), 4.14 (q, J=7.2 Hz, 2H), 1.39 (t, J=6.9 Hz, 3H).

Aufarbeitung

  1. customThe heat was removed
  2. customreaction
  3. stirringstirred at room temperature for 18 h
  4. customThe reaction was quenched with H2O (70 mL)
  5. extractionThe mixture was extracted with EtOAc (3×50 mL)
  6. washThe combined organics were washed with brine (2×50 mL)
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-ea0408dce8324c099e66ad0eedf8619d
Quelldatensatz
uspto-grants-2011_02
Patentnummer
US07879872B2

Verknüpfte Notizen

Wird geladen…