HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244305Generated: October 25, 2026
Tributylstannane → (E)-triethoxy(2-(tributylstannyl)vinyl)silane
https://huagongshe.com/reaction/244305
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Silane, triethoxyethynyl- | HCID 79778 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Product | (E)-triethoxy(2-(tributylstannyl)vinyl)silane | HCID 86668310 | 101.4% |
Reaction Steps
Tributyltin hydride (1.9 mL, 7.2 mmol, 1.0 equiv) and triethoxy(ethynyl)silane (1.5 g, 7.9 mmol, 1.1 equiv) were combined. AIBN (60 mg, 0.36 mmol, 0.05 equiv) was added and the resulting yellow solution was heated to 80° C. Upon reaching 80° C., the reaction exothermed to 104° C. The yellow solution was cooled back to 80° C. and stirred for 20 h. The reaction mixture was cooled to provide the title compound as a pale yellow oil (3.5 g, 99% crude yield): IR (thin film) 2957 (s), 2925 (s), 2873 (m), 2854 (m) cm−1; 1H NMR (400 MHz, CDCl3) δ 7.43 (d, J=24 Hz, 1H), 6.37 (d, J=24 Hz, 1H), 3.83 (q, J=7 Hz, 6H), 1.49 (m, 6H), 1.29 (m, 6H), 1.22 (t, J=7 Hz, 9 H), 0.82-0.92 (m, 15 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08658568B2 |
|---|
| Source dataset | uspto-grants-2014_02 |
|---|
| ORD ID | ord-48b6901412864ccaa3a78bc1e1853cf1 |
|---|
| Source note | uspto-grants-2014_02 |
|---|