HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributyltin Chloride → Diethyl 5-tributylstannyl-2-furanphosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Lithium cyclohexylisopropylamide | HCID 10877271 | — |
| Reactant | Phosphonic acid, 2-furanyl-, diethyl ester | HCID 12485182 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diethyl 5-tributylstannyl-2-furanphosphonate | HCID 22280515 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
A solution of diethyl 2-furanphosphonate (1 mmole, prepared as in Step C of Example 1) in THF was cooled at −78° C. and cannulated to a solution of lithium N-isopropyl-N-cyclohexylamide in THF at −78° C. over 15 min. The resulting mixture was stirred at −78° C. for 2 h and cannulated into a solution of tributyltin chloride (1 mmole) in THF at −78° C. over 20 min. The mixture was then stirred at −78° C. for 1 h, and at 25° C. for 12 h. Extraction and chromatography gave compound (14) as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06489476B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-0e892d62c3794766ab9ec88037809200 |
| Source note | uspto-grants-2002_12 |