Sodium Bicarbonate → 4-[3,5,6-Trimethyl-1,4-benzoquinon-2-yl(3-pyridyl)methyl]-alpha-methylcinnamic acid

HRID 232060Notes

Reaction equation

HRID 232060 reaction equation
[CH3:1][C:2]1[C:7](=[O:8])[C:6]([CH3:9])=[C:5]([CH3:10])[C:4](=[O:11])[C:3]=1[CH:12]([C:27]1[CH:28]=[N:29][CH:30]=[CH:31][CH:32]=1)[C:13]1[CH:26]=[CH:25][C:16]([CH:17]=[C:18]([CH3:24])[C:19]([O:21]CC)=[O:20])=[CH:15][CH:14]=1.C(=O)([O-])O.[Na+]>Cl>[CH3:1][C:2]1[C:7](=[O:8])[C:6]([CH3:9])=[C:5]([CH3:10])[C:4](=[O:11])[C:3]=1[CH:12]([C:27]1[CH:28]=[N:29][CH:30]=[CH:31][CH:32]=1)[C:13]1[CH:26]=[CH:25][C:16]([CH:17]=[C:18]([CH3:24])[C:19]([OH:21])=[O:20])=[CH:15][CH:14]=1

Participants

4

Procedure

Ethyl 4-[3,5,6-trimethyl-1,4-benzoquinon-2-yl-(3-pyridyl)methyl]-α-methylcinnamate, 1.2 g (2.8 mmol), was dissolved in 20 ml of concentrated hydrochloric acid, and refluxed by heating for 2 hours. After cooling, the reaction mixture was neutralized with a saturated aqueous solution of sodium hydrogen carbonate, and the resulting substance was extracted with ethyl acetate. The extract was washed with water and dried, and the solvent was evaporated off. The residue was purified with silica gel column chromatography (ethyl acetate-ethanol(9:1)), and recrystallized from ethyl acetate, to give 0.96 g (85.6%) of 4-[3,5,6-trimethyl-1,4-benzoquinon-2-yl(3-pyridyl)methyl]-α-methylcinnamic acid. The physical data are shown in Table 1.

Workup

  1. temperaturerefluxed
  2. temperatureby heating for 2 hours
  3. temperatureAfter cooling
  4. extractionthe resulting substance was extracted with ethyl acetate
  5. washThe extract was washed with water
  6. customdried
  7. customthe solvent was evaporated off
  8. customThe residue was purified with silica gel column chromatography (ethyl acetate-ethanol(9:1))
  9. customrecrystallized from ethyl acetate

Sources & evidence

ORD record
ord-fa778d7e406848e6a610454d0f383a50
Source dataset
uspto-grants-1989_07
Patent number
US04851413

Reaction notes

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