Potassium Hydroxide → HCID 22237485, compound

HRID 1281417Notes

Reaction equation

HRID 1281417 reaction equation
C([O:3][C:4](=[O:31])[C:5]1[CH:10]=[C:9]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([CH:17]=[O:18])[CH:12]=2)[C:8]([O:19][CH2:20][O:21][CH3:22])=[C:7]([C:23]2[CH:28]=[CH:27][CH:26]=[C:25]([CH:29]=[O:30])[CH:24]=2)[CH:6]=1)C.[OH-].[K+]>CO.Cl.O>[CH:17]([C:13]1[CH:12]=[C:11]([C:9]2[CH:10]=[C:5]([CH:6]=[C:7]([C:23]3[CH:28]=[CH:27][CH:26]=[C:25]([CH:29]=[O:30])[CH:24]=3)[C:8]=2[O:19][CH2:20][O:21][CH3:22])[C:4]([OH:31])=[O:3])[CH:16]=[CH:15][CH:14]=1)=[O:18]

Participants

6

Procedure

To a solution of 3,5-bis-(3-formylphenyl)-4-methoxymethoxybenzoic acid ethyl ester (960 mg, 2.12 mmol) in 3 mL MeOH was added 3 mL H2O and solid KOH (179 mg, 3.18 mmol). The reaction was refluxed for 5 to 6 hours then the cooled reaction mixture was diluted with 2N HCl and water. The aqueous solution was extracted with EtOAc (3×) and the combined organic layers were dried over Na2SO4. The solvent was removed in vacuo to give an oil that was flash chromatographed (10% MeOH:90% EtOAc) on silica gel. There yielded 650 mg of the desired acid along with some of the methyl ester of the desired acid. The methyl ester was resubjected to reaction conditions to give more of the desired acid for a total yield of 690 mg, 76.6%. 1H NMR (CDCl3) δ 2.63 (s, 3H); 4.19 (s, 2H); 7.65 (t, J=7.36 Hz, 2H); 7.87-7.95 (m, 4H); 8.06-8.26 (m, 4H); 10.10 (s, 2H).

Workup

  1. temperatureThe reaction was refluxed for 5 to 6 hours
  2. customthe cooled reaction mixture
  3. extractionThe aqueous solution was extracted with EtOAc (3×)
  4. dry with materialthe combined organic layers were dried over Na2SO4
  5. customThe solvent was removed in vacuo
  6. customto give an oil that
  7. customchromatographed (10% MeOH:90% EtOAc) on silica gel

Sources & evidence

ORD record
ord-02b34e0e403443dbb64415212005a3e3
Source dataset
uspto-grants-2002_09
Patent number
US06451827B2

Reaction notes

Loading…