HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphate → 3-Methylene-1-octene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphate | HCID 1061 | — |
| Reactant | Bromomethylbutadiene | HCID 548848 | — |
| Reactant | HCID 178418682 | HCID 178418682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Methylene-1-octene | HCID 11829433 | — |
Reaction Steps
n-bromosuccinimide (5.34 g) is added to a solution of isoprene (2.45 g) in carbon tetrachloride (100 ml), and the solution is stirred for 24 hours. The product and solvent are then fractionally distilled away from the succinimide, resulting in a partially concentrated solution of c-bromomethylbutadiene. The bromomethylbutadiene solution is chilled (-20° C.), and a 2N tetrahydrofuran solution of butylmagnesium bromide (15 ml) is then added. After stirring for 4 hours, the solution is treated with a 1 M phosphate buffer solution (pH 7). The organic layer is dried over sodium sulfate, and the reaction mixture is fractionally distilled to produce the product, 2-pentyl-1,3-butadiene, as a non-viscous liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05271864 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-7374aa8c98af4ea3874c2dce3e302978 |
| Source note | uspto-grants-1993_12 |