Hydrochloric Acid → HCID 18315473, compound
Reaction equation
[OH-].[Na+].[CH2:3]([C:10]1[N:14]([CH2:15][C:16]2[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][C:17]=2[Cl:23])[C:13]2[CH:24]=[C:25]([C:28]([O:30]CC)=[O:29])[CH:26]=[CH:27][C:12]=2[N:11]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.Cl>C(O)C>[CH2:3]([C:10]1[N:14]([CH2:15][C:16]2[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][C:17]=2[Cl:23])[C:13]2[CH:24]=[C:25]([C:28]([OH:30])=[O:29])[CH:26]=[CH:27][C:12]=2[N:11]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethanol (80 ml) and 10% sodium hydroxide aqueous solution (37 g) are added to 2-benzyl-1-(2,4-dichlorobenzyl)-6-ethoxycarbonylbenzimidazole (0.48 g) (example 12), and the solution is refluxed for 4 hours. After the reaction solution is cooled, its acidity is adjusted to pH 6 with 10% hydrochloric acid. The sediment is gathered, is washed with water, is dried under reduced pressure, and thus, 2-benzyl-6-carboxy-1-(2,4-dichlorobenzyl)benzimidazole (0.35 g) is obtained.
Workup
- temperaturethe solution is refluxed for 4 hours
- temperatureAfter the reaction solution is cooled
- washis washed with water
- customis dried under reduced pressure
Sources & evidence
- ORD record
- ord-d9d35bb8589b4aa08f55926a124ecc5e
- Source dataset
- uspto-grants-2001_04
- Patent number
- US06211177B1
Reaction notes
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