HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → HCID 14675643, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | HCID 14675642 | HCID 14675642 | — |
| Product | HCID 14675643 | HCID 14675643 | — |
Reaction Steps
A stirred mixture of 4.6 grams (0.0179 mole) of 4-chloro-1,1,2-trifluoro-1-dodecene (prepared as in Example 7) and 0.04 gram (0.0003 mole) of alpha, alpha-azobisisobutyronitrile is flushed with argon and 5.1 ml (0.019 mole) of tri-n-butyltin hydride is added dropwise. Upon completion of addition, the reaction mixture is stirred at ambient temperature for 16 hours. The reaction mixture is fractionally distilled under reduced pressure through a Vigreux column. The appropriate fractions are recombined and redistilled, again under reduced pressure and through a Vigreux column. The yield of 1,1,2-trifluoro-1-dodecene is 1.2 grams; b.p. 42°-45° C./0.45mm. The nmr spectrum is consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04997855 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-86f8b900ee4940f19aed142c730bc64a |
| Source note | uspto-grants-1991_03 |