HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → HCID 19613993, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,6-Dihydroxynaphthalene | HCID 93552 | — |
| Reactant | Diethyl (4-bromobutyl)phosphonate | HCID 14411016 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19613993 | HCID 19613993 | — |
Reaction Steps
1.34 g of KOH in ethanol were added dropwise to a mixture of 2,6-dihydroxynaphthalene (1.6g, 10 mmol) and diethyl(4-bromobutyl)phosphonate (6.0 g, 22 mmol) in ethanol, the mixture was left at room temperature for over night. The product was extracted with CH2Cl2. The CH2Cl2 solution was dried, leaving a brownish 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-e044e952609c43eab740f079d6d0c8e9 |
| Source note | uspto-grants-1999_11 |