Sodium Chloride → 1-(2-chloro-5-methoxyphenyl)ethanone

HRID 1169973Notes

Reaction equation

HRID 1169973 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

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

  1. additionTo the mixture was added
  2. distillationdistilled water (200 ml)
  3. extractionthe solution was extracted with dichloromethane (2×100 ml)
  4. dry with materialThe combined extracts were dried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by column chromatography (silica) with gradient elution, ethyl acetate
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-e16dcf7164f24acc9816c7945868afd3
Source dataset
uspto-grants-2010_11
Patent number
US07825149B2

Reaction notes

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