Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tributylstannane | HCID 5948 | 97.9% |
Reaction Steps
An apparatus similar to that in Example 2 was charged with 205 g tributyltin chloride and 50 ml toluene. During 35 min. there was added 110 ml Reagent T with the temperature controlled at 30° C. maximum by ice bath cooling. An hour after complete addition the toluene was distilled off. The residue, including a considerable amount of solid, was distilled under vacuum to give 179.5 g crude tributyltin hydride boiling 102°-110° C./5 mm. This was redistilled to give 158.9 g boiling 104°-106° C./5 mm and 8.0 g boiling 106°-116° C./5 mm, both showing only tributyltin hydride in the NMR spectrum, and a 12.5 g residue having the NMR spectrum of tributyltin chloride, for a 91.1% of theoretical yield of tributyltin hydride based on tributyltin chloride charged.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04282166 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-10cf620f2cc04b1a99e2f35dd0299930 |
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| Source note | uspto-grants-1981_08 |
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