HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromopyridine → Pyridine, 2-(trimethylstannyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Trimethyltin chloride | HCID 14016 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Pyridine, 2-(trimethylstannyl)- | HCID 11021057 | 51% |
Reaction Steps
A solution of 15.7 mL of 1.6 M n-butyllithium (25.1 mmol) in anhydrous ether (25 mL) was stirred under Ar at −78° C. and to this was added a solution of 2-bromopyridine (3.97 g, 25.1 mmol) in anhydrous ether (12.5 mL). The resulting orange solution was stirred for 2 h, and trimethyltin chloride in THF (26.0 mmol, 26 and, 1.0 M) added over 30 min. The reaction was stirred for 1 h at −78° C. then warmed to room temperature over 1 h, filtered and the filtrate evaporated. Distillation afforded 3.1 g (51%) of the title compound as a colorless liquid which solidified in the receiver flask. B.p. 65° C./2 mm Hg; Literature B.p. 75° C./4 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06380368B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-359b15264f76480d9bbaea1d4a3408bc |
| Source note | uspto-grants-2002_04 |