Reacción #1687655

ord-ad4abfbcf9ae429c9f79a37c477e5d63

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ExtracciónThe solution was extracted with CH2Cl2
  2. 2
    SecadoThe CH2Cl2 solution was dried
  3. 3
    Otroleaving a yellow solid
  4. 4
    OtroThe ester was purified by column chromatography
  5. 5
    workup.ADDITIONfollowed by addition of water
  6. 6
    LavadoThe bisphosphonic acid derivative was washed with CH2Cl2
  7. 7
    Filtraciónfiltered
  8. 8
    Otrocollected

Procedimiento

2,6-dihydroxyanthraquinone (1.19 g, 4.98 mmol) and diethyl(4-bromobutyl)phosphonate (3.0 g, 10 mmol) were heated at 60 ° C. in 5 ml DMF in the presence of 0.8 g of K2CO3 for 72 hours. The solution was extracted with CH2Cl2. The CH2Cl2 solution was dried, leaving a yellow solid. The ester was purified by column chromatography. The bisphosphonate ester was converted to the acid by overnight stirring with 4-fold excess of bromotrimethylsilane in dry dichloromethane followed by addition of water. The bisphosphonic acid derivative was washed with CH2Cl2, filtered and collected.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05976486uspto-grants-1999_11