HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyltin chloride → (Thiene-2,5-diyl)bis(trimethylstannane)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyltin chloride | HCID 14016 | — |
| Reactant | 2,3-Dibromothiophene | HCID 76590 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (Thiene-2,5-diyl)bis(trimethylstannane) | HCID 12841052 | 61% |
Reaction Steps
After 18.4 mL (30 mmol) of n-butyl lithium solution (n-BuLi, 1.63M in hexane) was added to a solution of 3.0 g (12.4 mmol) dibromothiophene in tetrahydrofuran (50 mL) at −50° C. under nitrogen atmosphere, the reaction was allowed to proceed for 30 minutes. To the mixture was added 5 g of trimethylstannyl chloride (SnMe3Cl, 25 mmol) and the reaction was continued at −50° C. for about 4˜5 hours. Next, the aqueous layer and organic layer were separated. The obtained organic layer was dried over a drying agent, and then solvents were removed. The resulting crude product was recrystallized from ether twice to afford 3.1 g (yield: 60%) of the title compound as a white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07030409B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-ee8fe7784fa4432ab563fe0d3f3b1936 |
| Source note | uspto-grants-2006_04 |