반응 #445296

ord-b36eca86bcb04671a0d8f648a4742b63

반응 방정식

[PH4+]
phosphonium
c1ccc(P(c2ccccc2)c2ccccc2)cc1
Triphenyl phosphine
COC(=O)CBr
methyl bromoacetate
[Na+].[OH-]
sodium hydroxide
COC(=O)C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
(methoxycarbonyl methyl)triphenylphosphonium bromide
COC(=O)C=P(c1ccccc1)(c1ccccc1)c1ccccc1
(methoxycarbonyl methylene) triphenyl phosphorane
수율 80.0%

반응 조건

온도
70°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooled
  2. 2
    여과filtered
  3. 3
    세척The residue was washed with benzene
  4. 4
    기타dried
  5. 5
    기타to give about 16 g
  6. 6
    여과The resulting precipitate was filtered off
  7. 7
    세척washed with water
  8. 8
    기타dried
  9. 9
    기타Crystallisation from ethyl acetate/petroleum spirit

실험 절차

Triphenyl phosphine (13 g.) was dissolved in dry benzene (60 ml.) and methyl bromoacetate (8.3 g.) was added dropwise. The solution was heated at 70° C., for 2 days, and then cooled and filtered. The residue was washed with benzene and dried to give about 16 g. of (methoxycarbonyl methyl)triphenylphosphonium bromide. The phosphonium salt (B 10 g.) was dissolved in water (250 ml.) and 5% aqueous sodium hydroxide was added dropwise with stirring until the solution became alkaline to litmus. The resulting precipitate was filtered off, washed with water and dried. Crystallisation from ethyl acetate/petroleum spirit gave (methoxycarbonyl methylene) triphenyl phosphorane as a colourless solid in about 80% yield.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04464391uspto-grants-1984_08