Potassium Iodide → HCID 54310319, compound
Reaction equation
[H-].[Na+].[C:3]([O:6][CH2:7][CH:8]([NH:18][C:19](=[O:21])[CH3:20])[CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=1)(=[O:5])[CH3:4].[CH2:22](Br)[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28].[I-].[K+]>CN(C)C=O.O1CCCC1.C(OCC)(=O)C.CCCCCC.O>[C:3]([O:6][CH2:7][CH:8]([NH:18][C:19](=[O:21])[CH3:20])[CH2:9][CH2:10][C:11]1[CH:12]=[CH:13][C:14]([O:17][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])=[CH:15][CH:16]=1)(=[O:5])[CH3:4]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 4
Procedure
To a suspension of sodium hydride (0.076 g) in dimethylformamide (1 ml) and tetrahydrofuran (1 ml), under a nitrogen atmosphere, a solution of 2-acetamido-4-(4-hydroxyphenyl)butyl acetate (0.51 g) in dimethylformamide (2 ml) was added and the mixture was stirred at room temperature for 50 minutes. Then, to the solution, heptyl bromide (0.35 g) and catalytic amount of potassium iodide were added and the mixture was stirred at 60° C. for 4 hours and 40 minutes. Then, the reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with a dilute aqueous sodium hydrogencarbonate solution and a saturated brine, dried over sodium sulfate and the solvent was distilled away under reduced pressure. The residue obtained was subjected to silica gel chromatography (eluent; ethyl acetate-hexane=4:1) to give the subject compound (0.30 g).
Workup
- stirringthe mixture was stirred at 60° C. for 4 hours and 40 minutes
- extractionextracted with ethyl acetate
- washThe extract was washed with a dilute aqueous sodium hydrogencarbonate solution
- dry with materiala saturated brine, dried over sodium sulfate
- distillationthe solvent was distilled away under reduced pressure
- customThe residue obtained
Sources & evidence
- ORD record
- ord-65577f555cf34c638202918cac83be0a
- Source dataset
- uspto-grants-2001_02
- Patent number
- US06187821B1
Reaction notes
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