Toluene → Methanefluorodiphosphonate

HRID 1157345Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1157345
[F:1][CH:2]([P:13](=[O:22])([O:18]C(C)C)[O:14]C(C)C)[P:3](=[O:12])([O:8]C(C)C)[O:4]C(C)C.C[Si](Br)(C)C.C1(C)C=CC=CC=1.C(N(CCCC)CCCC)CCC>ClCCCl.CN(C=O)C>[F:1][CH:2]([P:13](=[O:14])([OH:22])[OH:18])[P:3](=[O:4])([OH:12])[OH:8]

Komponenten

7

Reaktionsbedingungen

Temperatur
41 °C

Versuchsvorschrift

To a stirred solution of tetraisopropyl fluoromethylenediphosphonate (320 mg, 0.88 mmol) in 1,2-dichloroethane (5 mL) was added dropwise trimethylsilyl bromide (0.70 mL, 5.28 mmol). The resulting solution was stirred at 40-42° C. for 24 h and 3 mL of anhydrous toluene was added. The mixture was concentrated to dryness, and coevaporated with toluene once. The residue was redissolved in DMF (3 mL)/water (2 mL) mixture and concentrated. The residue was mixed with DMF (2 mL) and tributylamine (0.42 mL, 1.76 mmol) and then concentrated to dryness. The residue was coevaporated with anhydrous DMF two times. The resulting residue was dried in a vacuum oven at 30° C. overnight to give a slightly yellow residue (460 mg).

Aufarbeitung

  1. concentrationThe mixture was concentrated to dryness
  2. dissolutionThe residue was redissolved in DMF (3 mL)/water (2 mL) mixture
  3. concentrationconcentrated
  4. concentrationconcentrated to dryness
  5. customThe resulting residue was dried in a vacuum oven at 30° C. overnight

Quellen und Nachweise

ORD-Eintrag
ord-25983e843a934b708e885388ce9b3545
Quelldatensatz
uspto-grants-2010_10
Patentnummer
US07807653B2

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