HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → (E)-1-tri-n-butylstannyl-3-triethylsilyloxy-1-octene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 3-Triethylsilyloxy-1-octyne | HCID 12675346 | — |
| Product | (E)-1-tri-n-butylstannyl-3-triethylsilyloxy-1-octene | HCID 20442056 | — |
Reaction Steps
A solution of 20 g of 3-triethylsilyloxy-1-octyne, 150 mg of azobisisobutyronitrile, and 30 ml of tri-n-butyltin hydride is magnetically stirred under an argon atmosphere at 140° C. for 2 hours, (EXOTHERMIC), then cooled to ambient temperature. The excess tin hydride is removed by distillation (~70°/1.0 mm). The residue is purified by distillation to provide 36.5 g of the oil (bp 165° C. at 0.05 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04233231 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-08dd5583ae51474eba63d145237eb6e5 |
| Source note | uspto-grants-1980_11 |