Potassium Carbonate → HCID 68816406, compound

HRID 732505Notes

Reaction equation

HRID 732505 reaction equation
C[O:2][C:3](=[O:15])[C:4]1[CH:13]=[C:12]([OH:14])[CH:11]=[C:6]([C:7]([O:9][CH3:10])=[O:8])[CH:5]=1.C(=O)([O-])[O-].[K+].[K+].I[CH2:23][CH2:24][CH3:25].[OH-].[Na+]>CN(C=O)C.CO>[CH3:10][O:9][C:7](=[O:8])[C:6]1[CH:11]=[C:12]([O:14][CH2:23][CH2:24][CH3:25])[CH:13]=[C:4]([C:3]([OH:2])=[O:15])[CH:5]=1

Participants

7

Procedure

Heat commercially available 5-hydroxy-isophthalic acid dimethyl ester (1.0 g, 4.8 mmol), potassium carbonate (5.25 g, 38 mmol) and iodopropane (1.36 g, 8.0 mmol) in DMF (20 mL) at 70° C. for 8 h. Cool to room temperature, partition between ethyl acetate and 10% aqueous potassium carbonate. Wash the ethyl acetate layer with 1 N lithium chloride, saturated aqueous sodium chloride, dry (magnesium sulfate) and concentrate. Dissolve the residue in acetone (10 mL) and add a solution of NaOH (192 mg, 4.80 mmol) in methanol (2 mL). Stir at room temperature 16 h and concentrate. Partition between diethyl ether and 0.1 N citric acid, dry (magnesium sulfate) and concentrate to give the title compound.

Workup

  1. custompartition between ethyl acetate and 10% aqueous potassium carbonate
  2. washWash the ethyl acetate layer with 1 N lithium chloride, saturated aqueous sodium chloride
  3. dry with materialdry (magnesium sulfate)
  4. concentrationconcentrate
  5. dissolutionDissolve the residue in acetone (10 mL)
  6. concentrationconcentrate
  7. customPartition between diethyl ether and 0.1 N citric acid
  8. dry with materialdry (magnesium sulfate)
  9. concentrationconcentrate

Sources & evidence

ORD record
ord-dc6438ae10f24edcb974ea95c17370ba
Source dataset
uspto-grants-2009_09
Patent number
US07585885B2

Reaction notes

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