Boron tribromide → Benzofuran-5-ol

HRID 243572

Reaction equation

HRID 243572 reaction equation
C[O:2][C:3]1[CH:4]=[CH:5][C:6]2[O:10][CH:9]=[CH:8][C:7]=2[CH:11]=1.B(Br)(Br)Br>ClCCl>[O:10]1[C:6]2[CH:5]=[CH:4][C:3]([OH:2])=[CH:11][C:7]=2[CH:8]=[CH:9]1

Participants

4

Procedure

To a stirred solution of 5-methoxybenzofuran (1) (0.50 g, 3.38 mmol) in dichloromethane (15 mL), boron tribromide (16.87 mL, 16.87 mmol, 1M solution in dichloromethane) was added slowly at 0° C. The reaction mixture was warmed to room temperature and stirred for 4 hours. The reaction mixture was then cooled to 0° C., quenched with aqueous saturated NaHCO3 solution and extracted with dichloromethane (3×50 mL). The combined organic extracts were washed with brine (25 mL), dried over Na2SO4, and concentrated under reduced pressure to give compound (2) as an off white solid (300 mg) which was used in the next step without further purification.

Workup

  1. temperatureThe reaction mixture was then cooled to 0° C.
  2. customquenched with aqueous saturated NaHCO3 solution
  3. extractionextracted with dichloromethane (3×50 mL)
  4. washThe combined organic extracts were washed with brine (25 mL)
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-115a20a6d6054969b12c3810ee266b98
Source dataset
uspto-grants-2014_02
Patent number
US08653274B2

Linked notes

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