HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 1-Ferrocenyl-I-methyl-1,3-butadiene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | HCID 178466060 | HCID 178466060 | — |
| Reactant | HCID 178506586 | HCID 178506586 | — |
| Product | 1-Ferrocenyl-I-methyl-1,3-butadiene | HCID 131722479 | 99% |
Reaction Steps
According to the step flow described in Example 1, about 274 mg (1.20 mmole) of ferrocenyl methyl ketone react with 242 mg (2.0 mmole) of allyl bromide and 1.77 mmole of samarium diiodide in a temperature range of about 0° C. to room temperature to produce an oil-type 1-Ferrocenyl-1-methyl-1,3-butadiene (3b) with a weight of about 302 mg (1.19 mmole) and a yield of about 99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211392B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-d2cc93ecc2254f4f940d9c3d542781d0 |
| Source note | uspto-grants-2001_04 |