Water → 4-Chloro-2-iodophenol

HRID 2356615Notes

Reaction equation

HRID 2356615 reaction equation
B(Br)(Br)Br.[Cl:5][C:6]1[CH:11]=[CH:10][C:9]([O:12]C)=[C:8]([I:14])[CH:7]=1.O>ClCCl>[Cl:5][C:6]1[CH:11]=[CH:10][C:9]([OH:12])=[C:8]([I:14])[CH:7]=1

Participants

5

Conditions

Temperature
20 °C

Procedure

Boron tribromide (1349 g) was added to a solution of 4-chloro-2-iodoanisole (1025 g) in dichloromethane (10.3 L) under nitrogen at such a rate that the temperature remained at 0-5° C. The solution was then warmed to 20° C. and stirred for c. 19 h until the reaction was complete by HPLC. This organic solution was added to water (8.2 L) and the mixture was cooled to 5° C. to 10° C. DCM (770 ml) was added and the resulting biphasic mixture was then stirred at 5° C. for 15 min before being warmed to 22° C. and then finally stirred at 22° C. for 20 min before separating the phases. The separated organic phase was washed with aqueous saturated sodium bicarbonate (3.1 L), water (3.1 L) and then evaporated on a Buchi to give the title compound. (963.6 g)

Workup

  1. customremained at 0-5° C
  2. custom19 h
  3. temperaturethe mixture was cooled to 5° C. to 10° C
  4. stirringthe resulting biphasic mixture was then stirred at 5° C. for 15 min
  5. temperaturebefore being warmed to 22° C.
  6. stirringfinally stirred at 22° C. for 20 min
  7. custombefore separating the phases
  8. washThe separated organic phase was washed with aqueous saturated sodium bicarbonate (3.1 L), water (3.1 L)
  9. customevaporated on a Buchi

Sources & evidence

ORD record
ord-7dba6a08c6f341b0a524b87e9553c77b
Source dataset
uspto-grants-2010_07
Patent number
US07759369B2

Reaction notes

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