Sodium Chloride → 1-(2-chloro-5-methoxyphenyl)ethanone
Reaction equation
[B-](F)(F)(F)F.[B-](F)(F)(F)F.C1[N+]2([CH2:19][Cl:20])CC[N+](F)(CC2)C1.[Cl-].[Na+].[CH3:24][O:25][C:26]1[CH:27]=[C:28]([C:32](=[O:34])[CH3:33])C=[CH:30][CH:31]=1>C(#N)C>[Cl:20][C:19]1[CH:30]=[CH:31][C:26]([O:25][CH3:24])=[CH:27][C:28]=1[C:32](=[O:34])[CH3:33]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of SELECTFLUOR™(5.0 g, 14.1 mmol) and sodium chloride (825 mg, 14.1 mmol) in acetonitrile (200 ml), under nitrogen, was added 1-(3-methoxyphenyl)ethanone (1.94 ml, 14.1 mmol) and the reaction mixture was stirred at room temperature for 5 days. To the mixture was added distilled water (200 ml) and the solution was extracted with dichloromethane (2×100 ml). The combined extracts were dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography (silica) with gradient elution, ethyl acetate:cyclohexane [5:95 to 10:90]. The appropriate fractions were combined and concentrated to give the title compound (1.12 g).
Workup
- additionTo the mixture was added
- distillationdistilled water (200 ml)
- extractionthe solution was extracted with dichloromethane (2×100 ml)
- dry with materialThe combined extracts were dried (MgSO4)
- concentrationconcentrated in vacuo
- customThe residue was purified by column chromatography (silica) with gradient elution, ethyl acetate
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-e16dcf7164f24acc9816c7945868afd3
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07825149B2
Reaction notes
Loading…