HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → Tetraethyl (1-phenoxypropylidene)-bisphosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Tetraethyl (phenoxymethylene)-bisphosphonate | HCID 54483224 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tetraethyl (1-phenoxypropylidene)-bisphosphonate | HCID 53742288 | — |
Reaction Steps
Tetraethyl (phenoxymethylene)-bisphosphonate (1.14 g) was added to a suspension of 55% sodium hydride (0.15 g) in dimethylformamide (10 ml). After 45 minutes at room temperature, ethyl iodide (0.49 ml) was added, and the mixture was left overnight at room temperature, diluted with ethyl acetate and washed with 40% aqueous calcium chloride. The organic phase was dried and evaporated to leave an oil which was purified by chromatography on silica gel. The title compound was isolated as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04732998 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-d3e6e6ed0a0a4afe9c17dd9befff510f |
| Source note | uspto-grants-1988_03 |