Benzyl Bromide → HCID 3473490, compound

HRID 2228174Notes

Reaction equation

HRID 2228174 reaction equation
[CH2:1]([Mg]Cl)[CH3:2].[P:5]([O-:12])(OCC)OCC.[CH2:13](Br)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.O1CC[CH2:23][CH2:22]1>>[CH2:13]([P:5](=[O:12])([CH2:1][CH3:2])[CH2:22][CH3:23])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

Participants

5

Procedure

Under nitrogen atmosphere, to a solution of ethyl magnesium chloride in tetrahydrofuran (1.58M, 95 ml) was added diethyl phosphite (6.91 g) under ice-cooling, and the mixture was stirred at room temperature for 1 hour. To the mixture was added benzyl bromide (7.2 ml), and the mixture was refluxed for 4 hours. The reaction mixture was vigorously stirred and concentrated hydrochloric acid-ice was added to the mixture to stop the reaction. The mixture was extracted with diethylether and concentrated. To the residue was added chloroform, and the mixture was washed with water and concentrated under reduced pressure. The residue was separated and purified with column chromatography (ethyl acetate/ethanol=3:1→2:1) to give benzyldiethylphosphine oxide (1.45 g) as colorless crystals.

Workup

  1. temperaturecooling
  2. temperaturethe mixture was refluxed for 4 hours
  3. stirringThe reaction mixture was vigorously stirred
  4. customthe reaction
  5. extractionThe mixture was extracted with diethylether
  6. concentrationconcentrated
  7. additionTo the residue was added chloroform
  8. washthe mixture was washed with water
  9. concentrationconcentrated under reduced pressure
  10. customThe residue was separated
  11. custompurified with column chromatography (ethyl acetate/ethanol=3:1→2:1)

Sources & evidence

ORD record
ord-697d2630d2894adcaa487503e410eb5f
Source dataset
uspto-grants-2002_07
Patent number
US06413947B1

Reaction notes

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