Calcium Carbonate → 4-Hydroxymethyl-N-(2-methoxyphenyl)benzamide

HRID 2450

Reaction equation

HRID 2450 reaction equation
Cl[CH2:2][C:3]1[CH:19]=[CH:18][C:6]([C:7]([NH:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[O:16][CH3:17])=[O:8])=[CH:5][CH:4]=1.C(=O)([O-])[O-:21].[Ca+2].O1CCOCC1.O>C1COCC1>[OH:21][CH2:2][C:3]1[CH:19]=[CH:18][C:6]([C:7]([NH:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[O:16][CH3:17])=[O:8])=[CH:5][CH:4]=1

Participants

5

Procedure

4-Chloromethyl-N-(2-methoxyphenyl)benzamide (500 mg, 1.81 mmol) and precipitated calcium carbonate (970 mg, 9.7 mmol) were suspended in a dioxane-water (1:1) mixture solution (9 ml) and subjected to 25 hours of heating under reflux. After adding THF (25 ml) and filtering off the formed insoluble materials, the organic solvent was removed by evaporation. The thus obtained residue was extracted with ethyl acetate, and the resulting organic layer was washed with saturated brine and dried on anhydrous magnesium sulfate. After removing the solvent by evaporation, the resulting colorless solid material was purified by subjecting it to a silica gel column chromatography (ether:hexane=3:1), thereby obtaining 411 mg (88.3%) of the title compound in the form of colorless crystals.

Workup

  1. temperatureof heating
  2. temperatureunder reflux
  3. filtrationfiltering off the formed insoluble materials
  4. customthe organic solvent was removed by evaporation
  5. extractionThe thus obtained residue was extracted with ethyl acetate
  6. washthe resulting organic layer was washed with saturated brine
  7. dry with materialdried on anhydrous magnesium sulfate
  8. customAfter removing the solvent
  9. customby evaporation
  10. customthe resulting colorless solid material was purified

Sources & evidence

ORD record
ord-721576edcf544abdbf97d483a0968b14
Source dataset
uspto-grants-1998_03
Patent number
US05728835

Linked notes

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