Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoxazole | HCID 9228 | — |
| Reactant | Triethyltin bromide | HCID 17701 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Triethylstannylbenzoxazole | HCID 68978634 | — |
Reaction Steps
n-Butyllithium (1.6M, 6.0 mL, 9.57 mmol) was added to a solution of benzoxazole (950 mg, 7.98 mmol) in anhydrous ether (20 mL) stirred at −78° C. under nitrogen. After 10 min, triethylstannyl bromide (2.28 g, 7.98 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 the sub-title compound as a brown oily residue which was used directly without further purification for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07417050B2 |
|---|
| Source dataset | uspto-grants-2008_08 |
|---|
| ORD ID | ord-a6ccd87adc674d4f91f8b3b25741e14f |
|---|
| Source note | uspto-grants-2008_08 |
|---|