Cesium carbonate → 4-Chloro-2-(3-dimethylaminomethyl-2-propylphenoxy)-benzonitrile fumarate
Reaction equation
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4](F)[CH:3]=1.Br.[CH3:12][N:13]([CH2:15][C:16]1[C:17]([CH2:23][CH2:24][CH3:25])=[C:18]([OH:22])[CH:19]=[CH:20][CH:21]=1)[CH3:14].[C:26](=[O:29])([O-:28])[O-].[Cs+].[Cs+].[OH-:32].[Na+]>CN(C=O)C>[C:18]([OH:22])(=[O:32])/[CH:19]=[CH:20]/[C:26]([OH:28])=[O:29].[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([O:22][C:18]2[CH:19]=[CH:20][CH:21]=[C:16]([CH2:15][N:13]([CH3:14])[CH3:12])[C:17]=2[CH2:23][CH2:24][CH3:25])[CH:3]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
4-Chloro-2-fluorobenzonitrile (0.90 g, 5.8 mmol), 3-dimethylaminomethyl-2-propylphenol hydrobromide (1.58 g, 5.8 mmol) and cesium carbonate (3.94 g, 12.1 mmol) were heated with stirring in dry DMF (6 mL) at 50° C. for 18 h. The reaction mixture was cooled, poured into 0.1N sodium hydroxide solution and extracted with diethyl ether. The ether layer was separated, washed with 1N sodium hydroxide solution (1×), water (2×), brine (1×), and dried over MgSO4. After filtration, the solvent was removed in vacuo to give a yellow oil (1.77 g), which was purified by chromatography to yield 4-chloro-2-(3-dimethylaminomethyl-2-propylphenoxy)-benzonitrile (1.53 g, 81%) as a pale yellow oil. A small portion (100 mg) was converted into the fumarate salt (63 mg, 47%).
Workup
- temperatureThe reaction mixture was cooled
- extractionextracted with diethyl ether
- customThe ether layer was separated
- washwashed with 1N sodium hydroxide solution (1×), water (2×), brine (1×)
- dry with materialdried over MgSO4
- filtrationAfter filtration
- customthe solvent was removed in vacuo
Sources & evidence
- ORD record
- ord-c0102f27e81947789f2224ba25d61916
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07119122B2
Reaction notes
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