HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → HCID 20482698, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | {3-[(Prop-2-en-1-yl)oxy]phenyl}methanol | HCID 28065595 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20482698 | HCID 20482698 | 24% |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
To a solution of (3-allyloxy-phenyl)-methanol (Tetrahedron (2000), 56(13), 1873-1882) (1.07 g, 6.49 mmol) in THF (7 mls) at 3° C. was added carbon tetrabromide (2.69 g, 8.11 mmol) then triphenylphosphine (2.13 g, 8.11 mmol) in THF (2 mls). The reaction mixture was stirred at 5° C. for 1 hour. The reaction mixture was filtered and concentrated in vacuo. The residue was washed with pentane to give a yellow solid which was purified by column chromatography on silica gel, eluting with pentane:ethyl acetate, 100:0, to 95:5 to afford the title compound as a pale yellow oil in 24% yield, 350 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08486992B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-bee3443ecee146f3b0f8278866d8a4f6 |
| Source note | uspto-grants-2013_07 |