Phosphorus tribromide → 4-Bromo-1-(bromomethyl)-2-ethylbenzene

HRID 1438254Notes

Reaction equation

HRID 1438254 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8]O)=[C:4]([CH2:10][CH3:11])[CH:3]=1.P(Br)(Br)[Br:13]>C(Cl)(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][Br:13])=[C:4]([CH2:10][CH3:11])[CH:3]=1

Participants

4

Procedure

To a solution of (4-bromo-2-ethyl-phenyl)-methanol (7.9 g, 36.7 mmol) in anhydrous CHCl3 (122 mL) was added PBr3 (4.2 mL, 44.1 mmol). The resulting mixture was stirred at room temperature for 2 hours before it was quenched by the addition of water. The organic layer was washed with NaHCO3, brine and dried over MgSO4. The solvent was removed in vacuo and the residue was filtered through a pad of silica gel with 20% EtOAc in hexanes. The solvent was removed in vacuo to afford the desired product (8.4 g, 83%). 1H NMR (300 MHz, CDCl3): δ 1.29 (t, J=7.5 Hz, 3H), 2.71-2.78 (m, 2H), 4.48 (s, 2H), 7.17-7.20 (m, 1H), 7.29-7.32 (m, 1H), 7.36-7.38 (m, 1H).

Workup

  1. customwas quenched by the addition of water
  2. washThe organic layer was washed with NaHCO3, brine
  3. dry with materialdried over MgSO4
  4. customThe solvent was removed in vacuo
  5. filtrationthe residue was filtered through a pad of silica gel with 20% EtOAc in hexanes
  6. customThe solvent was removed in vacuo

Sources & evidence

ORD record
ord-5c4715fef6404cf48e44eac39cd390b6
Source dataset
uspto-grants-2009_11
Patent number
US07622605B2

Reaction notes

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