HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 1,3-Butadienylferrocene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Ferrocenecarboxyaldehyde | HCID 15184314 | — |
| Reactant | HCID 178450094 | HCID 178450094 | — |
| Reactant | HCID 178466060 | HCID 178466060 | — |
| Catalyst | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1,3-Butadienylferrocene | HCID 129665232 | — |
Reaction Steps
Ferrocenaldehyde or ferrocenyl methyl ketone and allyl bromide are reacted in an ether solvent and in the presence of magnesium metal as a catalyst. The liquid portion of the reaction mixture is introduced into a silica gel column, wherein the weak acidity of the silica gel is able to dehydrate the reaction intermediate 1-ferrocenyl-3-buten-1-ol product. The column is eluted with n-hexane, and after evaporating the solvent from the eluate collected, a purified ferrocenyl-1,3-butadiene product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06664409B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-1873e47b27344b03a5faf5cb04c75af6 |
| Source note | uspto-grants-2003_12 |