Water → 1-(2-Bromoethoxy)-4-iodobenzene

HRID 1280445Notes

Reaction equation

HRID 1280445 reaction equation
[I:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.C([O-])([O-])=O.[K+].[K+].[Br:15][CH2:16][CH2:17]Br.O>CN(C=O)C>[Br:15][CH2:16][CH2:17][O:8][C:5]1[CH:6]=[CH:7][C:2]([I:1])=[CH:3][CH:4]=1

Participants

6

Conditions

Temperature
50 °C

Procedure

To a stirring solution of 4-iodophenol (25 g, 110 mmol) and K2CO3 (31 g, 220 mmol) in DMF (250 mL) was added 1,2-dibromoethane (5 mL, 55 mmol) over a period of 1 hr. The solution was heated at 50° C. and stirred overnight under Ar. In order to complete the reaction additional reagents were added: 1,2-dibromoethane (20 mL, 220 mmol) and K2CO3 (6 g, 43 mmol) and the mixture was heated at 50° C. an additional 12 hours under Ar. Water was added and the reaction mixture was extracted with dichloromethane, dried over Na2SO4, filtered and the solvent evaporated under reduced pressure. The crude mixture was purified by silica gel chromatography eluted with 10% ethyl acetate in hexanes to give the title compound as a white solid (5.5 g, 17 mmol).

Workup

  1. additionwere added
  2. extractionthe reaction mixture was extracted with dichloromethane
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. customthe solvent evaporated under reduced pressure
  6. customThe crude mixture was purified by silica gel chromatography
  7. washeluted with 10% ethyl acetate in hexanes

Sources & evidence

ORD record
ord-7aa8a469c0ca4d77802b9f1dea9297fb
Source dataset
uspto-grants-2002_09
Patent number
US06451801B1

Reaction notes

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