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

HRID 54276

Reaktionsgleichung

Reaktionsgleichung von HRID 54276
[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

Komponenten

4

Edukt 2

HCID 3024DibromomethaneHCID 11776Triphenylphosphine

Produkt 1

HCID 2733422Phosphonium, (bromomethyl)triphenyl-, bromide (1:1)Ausbeute 78,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-4c6ba2453a834a448a547250555fd250
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05622954

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