Phosphorus tribromide → 5-Bromo-2-(bromomethyl)-1,3-difluorobenzene

HRID 576194Notes

Reaction equation

HRID 576194 reaction equation
[Br:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([CH2:9]O)=[C:4]([F:11])[CH:3]=1.[Br:12]P(Br)Br>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([CH2:9][Br:12])=[C:4]([F:11])[CH:3]=1

Participants

4

Procedure

To a solution of (4-bromo-2,6-difluorophenyl)methanol (2 g, 8.97 mmol) in DCM (80 mL) was added tribromophosphine (2.91 g, 10.76 mmol) at 0° C. The resulting mixture was stirred at rt. After LCMS analysis showed the starting material had disappeared, the mixture was washed with aq NaHCO3 (40 mL) and brine (30 mL). The organic layer was dried over Na2SO4, filtered and concentrated. The crude material was purified by silica column chromatography (PE/EA=5/1) to yield a colorless oil of 5-bromo-2-(bromomethyl)-1,3-difluorobenzene (1.6 g, 5.48 mmol, 61.2% yield): 1H NMR (400 MHz, CD3OD) δ 7.12 (d, J=6.8 Hz, 2H), 4.47 (s, 2H).

Workup

  1. washthe mixture was washed with aq NaHCO3 (40 mL) and brine (30 mL)
  2. dry with materialThe organic layer was dried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe crude material was purified by silica column chromatography (PE/EA=5/1)

Sources & evidence

ORD record
ord-a013fe7219fa44e8b8bf167ec3cc5774
Source dataset
uspto-grants-2015_05
Patent number
US09035063B2

Reaction notes

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