tert-Butyl methyl ether → 4-Bromo-2-(bromomethyl)-1-chlorobenzene

HRID 2296986Notes

Reaction equation

HRID 2296986 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:10])=[C:6]([CH:9]=1)[CH2:7]O.P(Br)(Br)[Br:12].COC(C)(C)C>C(OCC)C>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:10])=[C:6]([CH:9]=1)[CH2:7][Br:12]

Participants

5

Procedure

To a solution of 2.08 g (9.39 mol) of 5-bromo-2-chlorobenzylalcohol in 30 ml of dry diethyl ether was added dropwise 1.27 g (4.23 mmol) of phosphorous tribromide with ice-cooling. The mixture was stirred with ice-cooling for 3 hours and stirred at room temperature for 1.5 hours. To the reaction solution were added ice water and then tert-butyl methyl ether. The mixture was stirred for 30 minutes and separated. The organic layer was washed successively with an about 5% aqueous solution of sodium bicarbonate and water, then dried and concentrated. The solid residue (1.99 g) was subjected to silica gel column chromatography (eluted with n-hexane) to obtain 1.88 g of 5-bromo-2-chlorobenzylbromide as flocculent crystals.

Workup

  1. temperaturecooling
  2. temperaturecooling for 3 hours
  3. stirringstirred at room temperature for 1.5 hours
  4. stirringThe mixture was stirred for 30 minutes
  5. customseparated
  6. washThe organic layer was washed successively with an about 5% aqueous solution of sodium bicarbonate and water
  7. customdried
  8. concentrationconcentrated
  9. washThe solid residue (1.99 g) was subjected to silica gel column chromatography (eluted with n-hexane)

Sources & evidence

ORD record
ord-52763e9c490d4e37a18f758132707a05
Source dataset
uspto-grants-2002_12
Patent number
US06489487B1

Reaction notes

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