HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 1-(3-Bromoprop-1-yn-1-yl)-4-fluorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| 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 Conditions
| Temperature | 0 °C |
|---|
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 3 mmol/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 |
|---|---|
| Patent number | US08883826B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-be071408f1204465bad74f652f817451 |
| Source note | uspto-grants-2014_11 |