HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → trans-4-Difluoromethyl-4-trimethylsiloxy-1-tri-n-butylstannyl-1-octene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 4-Difluoromethyl-4-trimethylsiloxy-1-octyne | HCID 21764786 | — |
| Product | trans-4-Difluoromethyl-4-trimethylsiloxy-1-tri-n-butylstannyl-1-octene | HCID 21587526 | — |
Reaction Steps
a mixture of 13.0 g. of 4-difluoromethyl-4-trimethylsiloxy-1-octyne, 17.23 ml. of tri-n-butylstannane and 70 mg. of azobisisobutyronitrile is heated under nitrogen in an oil bath at 125°-135° C. for 2 hours. The reaction is cooled to room temperature and vacuum distilled through a short-path apparatus, giving, after a 5 ml. forerun, 35.6 g. of the product as on oil, containing a minor amount of the corresponding cis isomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04297516 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-91a2b8af17a94034b9a303d1e6901fbf |
| Source note | uspto-grants-1981_10 |