1-Bromo-3-chloropropane → HCID 18539271, compound

HRID 412895Notes

Reaction equation

HRID 412895 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[Cl:11])[NH:5][CH:6]=[O:7].Br[CH2:13][CH2:14][CH2:15][Cl:16].C(=O)([O-])[O-].[Cs+].[Cs+]>CC(C)=O>[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[Cl:11])[N:5]([CH2:13][CH2:14][CH2:15][Cl:16])[CH:6]=[O:7]

Participants

5

Procedure

To the mixture of 3,4-dichloro-N-formylaniline (133.0 g, 700 mmol), 1-bromo-3-chloropropane (132.3 g, 840 mmol) and acetone (700 mL) was added cesium carbonate (273.7 g, 840 mmol), and the mixture was stirred for under reflux. The reaction mixture was concentrated under reduced pressure, and to the concentrate was added ethyl acetate (500 mL). The organic layer was washed with water (300 mL) and saturated sodium chloride solution (100 mL×3), successively, dried over magnesium sulfate and concentrated under reduced pressure. The concentrate was subjected to column chromatography (silica gel 500 g×2, hexane/ethyl acetate=1/0 to 9/1 to 4/1), and the desired fraction was concentrated under reduced pressure to give the titled compound (143.5 g, 538 mmol, Yield 77%) as pale yellow oily substance.

Workup

  1. temperatureunder reflux
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. additionto the concentrate was added ethyl acetate (500 mL)
  4. washThe organic layer was washed with water (300 mL) and saturated sodium chloride solution (100 mL×3)
  5. dry with materialsuccessively, dried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. concentrationthe desired fraction was concentrated under reduced pressure

Sources & evidence

ORD record
ord-84868ee5baca4f238b2d3fc1520bbfcd
Source dataset
uspto-grants-2003_05
Patent number
US06562978B1

Reaction notes

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