HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → 1-Fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 1-Fluoro-1-phenylsulfonyl-3-methyl-3-(4-chlorophenyl)-1-butene | HCID 53860513 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | 1-Fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene | HCID 67632345 | — |
Reaction Steps
Under a nitrogen atmosphere, a stirring solution of 22.7 grams (0.067 mole) of 1-fluoro-1-phenylsulfonyl-3-methyl-3-(4-chlorophenyl)-1-butene, 42.0 grams (0.14 mole) of tributyltin hydride, and 0.5 gram (catalyst) of azobis-isobutyronitrile in 700 mL of cyclohexane is heated at reflux for about three hours. After this time the reaction mixture is cooled to ambient temperature, and 125 mL of silica gel is added. The mixture is concentrated under reduced pressure, and the residue is subjected to column chromatography. The product-containing fractions are combined and concentrated under reduced pressure, yielding 1-fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05696259 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-26be9e32081c4ba6a77a63b8dfa98cd8 |
| Source note | uspto-grants-1997_12 |