4-Bromo-o-xylene → Biphenyl

HRID 2072750Notes

Reaction equation

HRID 2072750 reaction equation
Br[C:2]1[CH:3]=[C:4]([CH3:9])[C:5](C)=[CH:6][CH:7]=1.[Mg]>O1CCCC1.[Cu](Cl)Cl>[C:9]1([C:4]2[CH:3]=[CH:2][CH:7]=[CH:6][CH:5]=2)[CH:4]=[CH:3][CH:2]=[CH:7][CH:6]=1

Participants

5

Procedure

A solution of 13.7 g of 4-bromo-o-xylene in 50 ml of dry tetrahydrofuran is added dropwise to a suspension of magnesium filings (1.95 g) in 50 ml of dry tetrahydrofuran in the course of 1 hour. After refluxing in an argon atmosphere for 2 hours, the mixture is cooled to room temperature and 9.4 g of anhydrous copper(II) chloride are added in portions. The mixture is poured onto ice-water and extracted twice with 100 ml of diethyl ether each time. The organic phase is washed with 2N hydrochloric acid and saturated sodium chloride solution. Drying with magnesium sulfate, evaporation and crystallisation of the residue from ethanol gives 2.9 g of biphenyl.

Workup

  1. temperatureAfter refluxing in an argon atmosphere for 2 hours
  2. additionThe mixture is poured onto ice-water
  3. extractionextracted twice with 100 ml of diethyl ether each time
  4. washThe organic phase is washed with 2N hydrochloric acid and saturated sodium chloride solution
  5. dry with materialDrying with magnesium sulfate, evaporation and crystallisation of the residue from ethanol

Sources & evidence

ORD record
ord-aa569917a9a94c82963ad5f0eb796b1c
Source dataset
uspto-grants-1990_04
Patent number
US04914182

Reaction notes

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