HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189080Generated: November 1, 2026
Carbon tetrabromide → 1-(3-Bromoprop-1-yn-1-yl)-4-fluorobenzene
https://huagongshe.com/reaction/1189080
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-(4-Fluorophenyl)prop-2-yn-1-ol | HCID 2782698 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(3-Bromoprop-1-yn-1-yl)-4-fluorobenzene | HCID 10560524 | 99.4% |
Reaction Steps
A solution of 3-(4-fluorophenyl)prop-2-yn-1-ol (1 g, 6.80 mmol) in DCM (13.6 mL) under N2 was cooled in a ice bath at 0° C. 2.70 g (8.2 mmol, loading 3mmol/g) of triphenylphosphine polymer supported was then added followed by 2.70 g (8.2 mmol) of carbon tetrabromide. The reaction mixture was stirred 15 min at 0° C. and warmed to room temperature for 90 min. After filtration through celite, the solvent was evaporated under reduce pressure. The crude product was purified by flash chromatography (prepacked 25 g silicagel column, DCM 100% as eluent) to afford 1.44 g of 1-(3-bromoprop-1-ynyl)-4-fluorobenzene as a yellow oil (Yield: 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08674106B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-98d06ac1f0c047d5a5f2f3d70d7d3e5b |
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| Source note | uspto-grants-2014_03 |
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