HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Methyl-2-(tributylstannyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 2-Bromo-3-methylpyridine | HCID 220832 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-Methyl-2-(tributylstannyl)pyridine | HCID 16427098 | 79% |
Reaction Steps
A solution (10 mL) of 2-bromo-3-methylpyridine (1.0 g) in tetrahydrofuran was cooled to −70° C., and a 1.6 mol/L solution (4.0 mL) of n-butyllithium in hexane was added dropwise. After stirring at the same temperature for 15 min, tributyltin chloride (2.2 g) was added dropwise. After further stirring for 1 hr, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate=19:1) to give the title compound as a colorless oil (yield 1.75 g, 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977488B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-d0ee0e761ee24ba19ca107a70e2202db |
| Source note | uspto-grants-2011_07 |