Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentane | HCID 8003 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Trimethyltin chloride | HCID 14016 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Stannane, trimethyl-2-thienyl- | HCID 11746949 | — |
Reaction Steps
To a solution of thiophene (2.1 g, 25.0 mmol) in anhydrous THF (50 mL) was added dropwise over 30 minutes at −38° C. t-butyllithium in pentane (1.6 M, 16.0 mL, 25.6 mmol). The solution was stirred for 1 h at −38° C. and then cooled to −78° C. Trimethyltin chloride in THF (1 M, 25.3 mL, 25.3 mmol) was added dropwise over 30 min. The reaction was then stirred for 2 h at −78° C. and then for 15 h at r.t. The solvent was evaporated and the resulting yellow solid was taken up in other, washed with water and dried Na2SO4 and then evaporated to give a light brown liquid which solidified on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06875593B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-afba8c43295f4fbaa3a1cd1f053a1d5d |
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| Source note | uspto-grants-2005_04 |
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