Hydrochloric Acid → HCID 86588524, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9]([CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]([CH2:31][CH2:32][CH2:33][C:34]([F:40])([F:39])[C:35]([F:38])([F:37])[F:36])([C:26]([O:28]CC)=[O:27])[C:21]([O:23]CC)=[O:22])=[C:8]([C:41]1[CH:46]=[CH:45][C:44]([O:47][CH3:48])=[CH:43][CH:42]=1)[CH:7]=[CH:6]2.[OH-].[Na+].O.Cl>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9]([CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]([CH2:31][CH2:32][CH2:33][C:34]([F:40])([F:39])[C:35]([F:38])([F:37])[F:36])([C:26]([OH:28])=[O:27])[C:21]([OH:23])=[O:22])=[C:8]([C:41]1[CH:46]=[CH:45][C:44]([O:47][CH3:48])=[CH:43][CH:42]=1)[CH:7]=[CH:6]2Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Diethyl 2-[7-[6-methoxy-2-(4-methoxyphenyl)napht-1-yl]heptyl]-2-(4,4,5,5,5-pentafluoropentyl)malonate (1.02 g, 1.5 mmol) was dissolved in ethanol (10 ml). To this solution, sodium hydroxide (1.2 g, 30 mmol) and water (1 ml) were added, and the resulting mixture was heated under reflux for 3 hours. Dilute hydrochloric acid was added to the reaction mixture, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous sodium sulfate. The solvent was distilled off to give 2-[7-[6-methoxy-2-(4-methoxyphenyl)napht-1-yl]heptyl]-2-(4,4,5,5,5-pentafluoropentyl)malonic acid (1.0 g).
Workup
- temperaturethe resulting mixture was heated
- temperatureunder reflux for 3 hours
- extractionwas then extracted with ethyl acetate
- washThe organic layer was washed with saturated aqueous sodium chloride
- dry with materialdried over anhydrous sodium sulfate
- distillationThe solvent was distilled off
Sources & evidence
- ORD record
- ord-deec914f59df4cddbd0451c919234114
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07196081B2
Reaction notes
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