1-Bromo-2-Chloroethane → 1-(2-Chloroethoxy)-4-iodobenzene
Reaction equation
[I:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[Cs+].[Cs+].Br[CH2:16][CH2:17][Cl:18]>C(#N)C>[Cl:18][CH2:17][CH2:16][O:8][C:5]1[CH:6]=[CH:7][C:2]([I:1])=[CH:3][CH:4]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
To a solution of 4-iodophenol (1.0 g) in acetonitrile (10 mL), cesium carbonate (3.0 g) and 1-bromo-2-chloroethane (0.8 g) were added and the mixture was heated to 100° C., at which it was stirred for 4 hours. Additional 1-bromo-2-chloroethane (1.0 g) was further added and stirred at 100° C. for 4 hours. The reaction mixture was cooled to room temperature and filtered to remove insoluble materials, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by NH-type silica gel column chromatography (eluting solvent: n-hexane:ethyl acetate=11:1) to give the titled compound (0.87 g, 68%) as a yellow oil.
Workup
- stirringstirred at 100° C. for 4 hours
- temperatureThe reaction mixture was cooled to room temperature
- filtrationfiltered
- customto remove insoluble materials
- concentrationthe filtrate was concentrated under reduced pressure
- customThe resulting residue was purified by NH-type silica gel column chromatography (eluting solvent: n-hexane:ethyl acetate=11:1)
Sources & evidence
- ORD record
- ord-71fc18e1079349acbcd9a0cc3db64d66
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07888354B2
Reaction notes
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