HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributyltin Chloride → 4-Tri-n-butylstannylfuran-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 4-Bromofuran-2-carbonitrile | HCID 21986220 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Tri-n-butylstannylfuran-2-carbonitrile | HCID 68615245 | 53% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
n-Butyllithium (1.6M, 3.7 mL, 5.93 mmol) was added to a solution of 4-bromofuran-2-carbonitrile (850 mg, 4.94 mmol) in anhydrous ether (15 mL) stirred at −78° C. under nitrogen. After 10 min, tri-n-butylstannyl chloride (1.61 g, 4.94 mmol) was added, then the reaction mixture was allowed to warm to room temperature, and stirred for another 1 h. The mixture was quenched, and washed with 1N sodium hydroxide, dried through MgSO4, and then the solvent was evaporated to give a brown oily residue. Purification by flash chromatography using a gradient of ammoniated methanol in chloroform gave the sub-title compound as a yellow oil (1.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07417049B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-6310cf939366470baa4f36fbe280f5ee |
| Source note | uspto-grants-2008_08 |