Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | HCID 101337817 | HCID 101337817 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Allyl bromide | HCID 7841 | — |
| Product | HCID 86652237 | HCID 86652237 | — |
Reaction Steps
(Trimethylsilylethynyl)diisopropylsilane (14 g, 66 mmol) and allyl bromide (˜40 mL) were added to a round-bottom flask equipped with a stir-bar. A septum and bubbler were attached and the solution was purged with N2 for 15 min. PdCl2 (0.06 g, 0.3 mmol, 0.5 mol %) was added and the reaction was heated at 60° C. for 3 hours, or until analysis by GC-MS showed complete conversion to the bromide. After removing the reaction from the heat, pentane (50 mL) was added and the solution was chilled for 20 min. The PdCl2 was removed by filtration through a fine fitted funnel, then solvent was removed using a rotary evaporator, yielding 18.8 g of (trimethylsilylethynyl)diisopropylbromosilane as a light brown liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809568B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-df19251f67504e879297feadbfe5ceec |
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| Source note | uspto-grants-2014_08 |
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