HuagongsheHuagongshe Chemistry Print Report · For research reference only
Vinyl Chloride → HCID 21501105, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Vinyl Chloride | HCID 6338 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 21501148 | HCID 21501148 | — |
| Reactant | HCID 178461836 | HCID 178461836 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21501105 | HCID 21501105 | — |
Reaction Steps
A solution of 6-[4-(t-butoxy)pentyl]-tetrahydropyran-2-ol (5 g.) in tetrahydrofuran (50 ml.) was added within 30 minutes at 5° to a solution of vinyl magnesium chloride in tetrahydrofuran, prepared from magnesium (2.0 g.) and 4 g. of vinyl chloride, dissolved in tetrahydrofuran (50 ml.). After stirring overnight at room temperature, the reaction solution was treated with ammonium chloride-ice and then extracted with chloroform (3 times, each time 100 ml.). The organic phase was washed with water, dried and evaporated in vacuo giving crude 3,7-dihydroxy-11-(t-butoxy)-dodec-1-ene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03989724 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-e17621cbc7144e43826f644ecd5832e7 |
| Source note | uspto-grants-1976_11 |