Potassium Hydroxide → HCID 15754281, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:22]=[C:23]([Cl:26])[C:24]=1[F:25])[C:5]([N:8]([CH2:18][C:19](=O)[CH3:20])[C:9](=[O:17])[CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)([CH3:7])[CH3:6].[OH-].[K+]>C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]([CH:22]=[C:23]([Cl:26])[C:24]=1[F:25])[C:5]([N:8]1[CH2:18][C:19]([CH3:20])=[C:10]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:9]1=[O:17])([CH3:7])[CH3:6]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4.0 g (0.01 mol) of N-(3,5-dichloro-4-fluoro-α,α-dimethylbenzyl)-N-(2-oxopropyl)phenylacetamide prepared in accordance with the method of Reference Example 8, was dissolved in 50 ml of ethyl alcohol, and 0.5 g (0.009 mol) of potassium hydroxide powder was added thereto. The mixture was refluxed under heating for 10 minutes. Then, the solvent was distilled off under reduced pressure, and water was added thereto and extracted with ethyl acetate. The ethyl acetate layer was dried over an hydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure, followed by purification by silica gal column chromatography (n-hexane/ethyl acetate) to obtain 2.5 g (yield: 67.5%) of the desired compound as colorless crystals.
Workup
- temperatureThe mixture was refluxed
- temperatureunder heating for 10 minutes
- distillationThen, the solvent was distilled off under reduced pressure, and water
- additionwas added
- extractionextracted with ethyl acetate
- dry with materialThe ethyl acetate layer was dried over an hydrous magnesium sulfate
- distillationthe solvent was distilled off under reduced pressure
- customfollowed by purification by silica gal column chromatography (n-hexane/ethyl acetate)
Sources & evidence
- ORD record
- ord-84948551ffe94d46b2c3cb16130709d6
- Source dataset
- uspto-grants-1991_12
- Patent number
- US05076834
Reaction notes
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