Toluene → HCID 66961793, compound
Reaction equation
[C:1]1([CH3:7])C=CC=CC=1.[N:8]1([C:13]2[C:20]([O:21][CH3:22])=[CH:19][CH:18]=[CH:17][C:14]=2C=O)[CH:12]=[CH:11][N:10]=[CH:9]1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1.O.[C:36](=O)([OH:38])[O-:37].[Na+]>C(OCC)(=O)C.C(O)CO>[O:37]1[CH2:7][CH2:1][O:38][CH:36]1[C:18]1[CH:17]=[CH:14][C:13]([N:8]2[CH:12]=[CH:11][N:10]=[CH:9]2)=[C:20]([O:21][CH3:22])[CH:19]=1Participants
Procedure
To a toluene (70 mL) solution of 4-(1H-imidazol-1-yl-3-methoxybenzaldehyde (4.3 g) and ethylene glycol (6.5 g), para-toluenesulfonic acid monohydrate (4.8 g) was added, Dean-Stark equipment was attached and heat-refluxing was carried out for 4 hours. After allowing cool the reaction mixture to room temperature, a saturated sodium bicarbonate water and ethyl acetate were added, and the organic layer was partitioned. The organic layer was washed with a saturated salt solution and concentrated under reduced pressure after dried over anhydrous magnesium sulfate. The residue was purified by silica gel column chromatography (elution solvent:hexane-ethyl acetate system), and 3.15 g of the title compound was obtained. The physical properties of the compound are as follows.
Workup
- temperatureheat-refluxing
- customthe organic layer was partitioned
- washThe organic layer was washed with a saturated salt solution
- concentrationconcentrated under reduced pressure
- dry with materialafter dried over anhydrous magnesium sulfate
- customThe residue was purified by silica gel column chromatography (elution solvent:hexane-ethyl acetate system)
Sources & evidence
- ORD record
- ord-f6251304ade846deaa30d800ec3f68e6
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07667041B2
Reaction notes
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