Boron tribromide → 4-Bromo-3-isopropylphenol

HRID 1597024Notes

Reaction equation

HRID 1597024 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8]C)=[CH:4][C:3]=1[CH:10]([CH3:12])[CH3:11].B(Br)(Br)Br>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][C:3]=1[CH:10]([CH3:12])[CH3:11]

Participants

4

Conditions

Temperature
-78 °C

Procedure

To a solution of 1-bromo-2-isopropyl-4-methoxy-benzene (Intermediate 143, 2.20 g, 9.60 mmols) in 50 mL CH2Cl2 at −78° C. was added BBr3 (4.81 g, 19.2 mmols; 19.2 mL of a 1M solution in CH2Cl2). After stirring for 3 hours at −78° C. the solution was warmed to 0° C. for 3 hours and then at 25° C. for 1 hour before being quenched with H2O. The mixture was diluted with Et2O and washed with H2O and saturated aqueous NaCl, dried (Na2SO4) and concentrated under reduced pressure. Column chromatography (2.5-10% EtOAc-hexanes) afforded the title compound as a colorless oil.

Workup

  1. temperaturewas warmed to 0° C. for 3 hours
  2. customat 25° C. for 1 hour before being quenched with H2O
  3. additionThe mixture was diluted with Et2O
  4. washwashed with H2O and saturated aqueous NaCl
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-cdd2b862f03c41af8ffb97014a009742
Source dataset
uspto-grants-2001_09
Patent number
US06291677B1

Reaction notes

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