HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzothiazole → 2-(Tributylstannyl)-1,3-benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzothiazole | HCID 7222 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(Tributylstannyl)-1,3-benzothiazole | HCID 3762392 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
n-Butyllithium (1.6M, 10 mL, 15.98 mmol) was added to a solution of benzothiazole (1.80 g, 13.3 mmol) in anhydrous ether (30 ml) stirred at −78° C. under nitrogen. After 10 min, tri-n-butylstannyl chloride (4.33 g, 13.31 mmol) was added, then the solution 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, filtered, and evaporated to give the sub-title compound as a brown oily residue (5.0 g), which was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07417050B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-9890acb71d2f4827bd88e2b812d65f4c |
| Source note | uspto-grants-2008_08 |