HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244303Generated: October 27, 2026
Tributylstannane → (E)-trimethyl(2-(tributylstannyl)vinyl)silane
https://huagongshe.com/reaction/244303
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Product | (E)-trimethyl(2-(tributylstannyl)vinyl)silane | HCID 10949136 | 98.5% |
Reaction Steps
Tributyltin hydride (2.0 mL, 7.3 mmol, 1.0 equiv) and ethynyltrimethylsilane (2.1 mL, 15 mmol, 2.0 equiv) were combined, AIBN (60 mg, 0.36 mmol, 0.05 equiv) was added, and the resulting colorless neat solution was heated to 80° C. Upon heating, the reaction exothermed to −110° C. The reaction mixture was cooled back to 80° C. and stirred for 20 h. The reaction mixture was cooled to 23° C. to afford the crude title compound as a pale yellow oil (2.8 g, 99% crude yield): 1H NMR (400 MHz, CDCl3) δ 6.96 (d, J=22.5 Hz, 1H), 6.60 (d, J=22.5 Hz, 1H), 1.44-1.54 (m, 6H), 1.23-1.35 (m, 6H), 0.82-0.91 (m, 15H), 0.03 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658568B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-2e11b529c474474284eecc861e5e5d70 |
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| Source note | uspto-grants-2014_02 |
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