Dibromomethane → Phosphonium, (bromomethyl)triphenyl-, bromide (1:1)

HRID 54276

Reaction equation

HRID 54276 reaction equation
[C:1]1([P:7]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br:20][CH2:21][Br:22]>C1(C)C=CC=CC=1>[Br-:20].[Br:22][CH2:21][P+:7]([C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Participants

4

Reactant 2

HCID 3024DibromomethaneHCID 11776Triphenylphosphine

Product 1

HCID 2733422Phosphonium, (bromomethyl)triphenyl-, bromide (1:1)Yield 78.3%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

Under a nitrogen atmosphere, a stirred solution of 215.0 grams (0.82 mole) of triphenylphosphine and 115 mL (1.64 moles) of dibromomethane in 600 mL of toluene was heated at reflux for about eight hours. After this time a solid was collected by filtration. The filtrate was again heated to reflux where it stirred for an additional eight hours. The mixture was cooled and additional solid was collected by filtration. The two solids were combined, yielding about 280 grams of bromomethyl triphenylphosphonium bromide.

Workup

  1. temperatureat reflux for about eight hours
  2. filtrationAfter this time a solid was collected by filtration
  3. temperatureThe filtrate was again heated
  4. temperatureto reflux where it
  5. temperatureThe mixture was cooled
  6. filtrationadditional solid was collected by filtration

Sources & evidence

ORD record
ord-4c6ba2453a834a448a547250555fd250
Source dataset
uspto-grants-1997_04
Patent number
US05622954

Linked notes

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