HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → E-1-Tri-n-butylstannyl-4-methyl-4-tri-methylsilyloxy-7-oxa-1-octene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 4-Methyl-4-trimethylsilyloxy-7-oxa-1octyne | HCID 12786230 | — |
| Product | E-1-Tri-n-butylstannyl-4-methyl-4-tri-methylsilyloxy-7-oxa-1-octene | HCID 12786231 | — |
Reaction Steps
To a stirred solution of 15 g. (0.069 moles) of 4-methyl-4-trimethylsilyloxy-7-oxa-1octyne and 75 mg. of azobisisobutyronitrile is added dropwise, under nitrogen atmosphere, 21.1 g. (0.073 moles) of tri-n-butyltin hydride. The solution is stirred at 130°-135° C. for 11/2 hours, then cooled to ambient temperature. Distillation provides 29 g. (86%) of product as a colorless oil; b.p. 165°-167° C. (0.25 mm.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04297516 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-1d20a628ce4f40c48c5c0f93c72ddc7e |
| Source note | uspto-grants-1981_10 |