HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophene → 2-(Tri-n-butylstannyl)thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Tri-n-butylstannyl)thiophene | HCID 2779373 | 55.8% |
Reaction Steps
Thiophene (2.0 g, 12 mmol) was dissolved in anhydrous THF (20 mL) and n-BuLi (9.52 mL, 23.8 mmol, 2.5 M in hexane) slowly added at −30° C. under nitrogen flow. After stirring for 1 hour, tributyltin chloride (7.75 mL, 23.8 mmol) was added. After heating to room temperature, followed by stirring for 3 hours, the reaction was terminated. The produced compound was extracted with n-hexane and distilled water, dried with anhydrous MgSO4 and filtered under reduced pressure. The final product tributyl-2-thienylstannane (2.5 g, yield: 46%) was obtained by column chromatography (neutral alumina, n-hexane). The product was used in the next step after removing the solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08519087B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-bf304fdb6fde4673b4096fc2d1da5f6e |
| Source note | uspto-grants-2013_08 |