Potassium Carbonate → HCID 57934053, compound

HRID 2424188Notes

Reaction equation

HRID 2424188 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][CH:12]=2)=[C:7]([OH:9])[CH:8]=1.F[C:20]1[CH:27]=[CH:26][C:23]([CH:24]=[O:25])=[CH:22][CH:21]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C(=O)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][CH:12]=2)=[C:7]([CH:8]=1)[O:9][C:20]1[CH:27]=[CH:26][C:23]([CH:24]=[O:25])=[CH:22][CH:21]=1

Participants

5

Procedure

The title compound was synthesized by referring to Synthesis, 1991, (1), 63. To a solution of 5-methoxy-2-(4-methoxybenzyl)phenol (1.9 g) in N,N-dimethylacetamide (6 ml) was added 4-fluorobenzaldehyde (960 mg) and potassium carbonate (1.3 g), and the solution was refluxed for 1 hour and 10 minutes. The solution was extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (2.0 g).

Workup

  1. customThe title compound was synthesized
  2. customby referring to Synthesis, 1991, (1), 63
  3. temperaturethe solution was refluxed for 1 hour and 10 minutes
  4. extractionThe solution was extracted with ethyl acetate
  5. washsequentially washed with water and brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customthe solvent was evaporated in vacuo
  8. customThe residue was purified by silica gel column chromatography (hexane-ethyl acetate system)

Sources & evidence

ORD record
ord-cb6c5cca324349a1b982dbfce364a49b
Source dataset
uspto-grants-2011_06
Patent number
US07960412B2

Reaction notes

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