Reacción #1687655
ord-ad4abfbcf9ae429c9f79a37c477e5d63
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1ExtracciónThe solution was extracted with CH2Cl2
- 2SecadoThe CH2Cl2 solution was dried
- 3Otroleaving a yellow solid
- 4OtroThe ester was purified by column chromatography
- 5workup.ADDITIONfollowed by addition of water
- 6LavadoThe bisphosphonic acid derivative was washed with CH2Cl2
- 7Filtraciónfiltered
- 8Otrocollected
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.