HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387659Generated: November 1, 2026
Carbon tetrabromide → HCID 20482698, compound
https://huagongshe.com/reaction/2387659
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 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 |
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| Patent number | US08268881B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-1c8d61c1235546bbb3432c0aa0819e1d |
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| Source note | uspto-grants-2012_09 |
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