HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716981Generated: November 2, 2026
Hexane → Stannane, [2,2'-bithiophen]-5-yltrimethyl-
https://huagongshe.com/reaction/1716981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Trimethyltin chloride | HCID 14016 | — |
| Reactant | 2,2'-Bithiophene | HCID 68120 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Stannane, [2,2'-bithiophen]-5-yltrimethyl- | HCID 11034846 | 64% |
Reaction Steps
To a 3-necked flask equipped with a glass stopper, rubber septum and a nitrogen inlet was added 2,2′-bithiophene (10 g, 60.1 mmol) and anhydrous THF (100 mL). The dark (green) solution was cooled to 0° C. A 2.5 M solution of n-BuLi in hexane (26.4 mL, 66 mmol) was added via syringe. The reaction mixture was then stirred at 25° C. for 1.5 hours. The mixture was cooled to −78° C. and a 1.0 M solution of trimethylstannyl chloride in THF (66 mL, 66 mmol) was added slowly via syringe. The reaction mixture was allowed to warm to 25° C. and was stirred overnight. THF was removed in vacuo and the residue was dissolved in pentane (200 mL). The pentane layer was washed with water (3×200 mL), dried over MgSO4, and the pentane was removed in vacuo to yield a green oil. The oil was purified by vacuum distillation (118-120° C., 0.6 mmHg) to yield 12.5 g (64%) of product MS=330.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803885B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-432b9a573a294b69a32f61bf78aea977 |
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| Source note | uspto-grants-2010_09 |
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