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

HRID 2387061Notes

Reaction equation

HRID 2387061 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, 3 H), 2.71-2.78 (m, 2 H), 4.48 (s, 2H), 7.17-7.20 (m, 1H), 7.29-7.32 (m, 1 H), 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-fbd7b5c06c4e4687a8eb83881909a3e2
Source dataset
uspto-grants-2012_09
Patent number
US08268835B2

Reaction notes

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