Triphenylphosphine → 1-(2-Bromoethyl)-4-methoxybenzene

HRID 1814460Notes

Reaction equation

HRID 1814460 reaction equation
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([CH2:7][CH2:8]O)=[CH:5][CH:4]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Br:31]N1C(=O)CCC1=O>C(Cl)Cl>[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([CH2:7][CH2:8][Br:31])=[CH:5][CH:4]=1

Participants

5

Reactant 3

HCID 11776TriphenylphosphineHCID 67184N-bromobutanimideHCID 697054-Methoxyphenethyl alcohol

Product 1

HCID 844271-(2-Bromoethyl)-4-methoxybenzeneYield 71.2%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

4-Methoxyphenethyl alcohol (50 g) and triphenylphosphine (103 g) were dissolved in methylene chloride (600 ml), followed by the addition of N-bromosuccinimide (70 g) in small portions under ice-cooling, and the resulting mixture was stirred at room temperature for 30 min. The reaction mixture was evaporated, and to the resulting residue was added hexane. The insoluble matters were filtered off, while the resulting filtrate was evaporated, to give the title compound as a colorless oil (50.32 g, yield: 71%).

Workup

  1. temperaturecooling
  2. customThe reaction mixture was evaporated
  3. additionto the resulting residue was added hexane
  4. filtrationThe insoluble matters were filtered off, while the resulting filtrate
  5. customwas evaporated

Sources & evidence

ORD record
ord-fd619eb48f994c9aa02079f602e31a48
Source dataset
uspto-grants-2005_04
Patent number
US06875761B2

Reaction notes

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