HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Dihydroxyanthraquinone → HCID 53655413, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Dihydroxyanthraquinone | HCID 6776 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diethyl (4-bromobutyl)phosphonate | HCID 14411016 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53655413 | HCID 53655413 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05976486 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-ad4abfbcf9ae429c9f79a37c477e5d63 |
| Source note | uspto-grants-1999_11 |