Sodium Hydroxide → HCID 14800668, compound
Reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][O:12][C:13]1[CH:29]=[CH:28][C:16]([CH2:17][C:18]2[CH:19]=[C:20]([CH:25]=[CH:26][CH:27]=2)[C:21]([O:23]C)=[O:22])=[CH:15][CH:14]=1.[OH-].[Na+]>C(O)C>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][O:12][C:13]1[CH:29]=[CH:28][C:16]([CH2:17][C:18]2[CH:19]=[C:20]([CH:25]=[CH:26][CH:27]=2)[C:21]([OH:23])=[O:22])=[CH:15][CH:14]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Methyl 3-(4-(2-quinolinylmethyloxy)benzyl)benzoate (0.05 mol) is heated at reflux in a 9:1 mixture of ethanol and 0.5N aqueous NaOH (450 ml). After several hours the clear reaction is evaporated. The solid residue is taken up in water and acidified. The resulting crystalline product is isolated by filtration and dried by suction with a rubber dam to obtain 3-(4-(2-quinolinylmethyloxy)benzyl)benzoic acid.
Workup
- customAfter several hours the clear reaction
- customis evaporated
- customThe resulting crystalline product is isolated by filtration
- customdried by suction with a rubber dam
Sources & evidence
- ORD record
- ord-1eb0a02f7d324e47b6af0d493ef3a471
- Source dataset
- uspto-grants-1990_04
- Patent number
- US04920133
Reaction notes
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