HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 3-(2-Bromoethyl)-5-fluorobenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-(5-Fluorobenzofuran-3-yl)ethanol | HCID 18184294 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(2-Bromoethyl)-5-fluorobenzofuran | HCID 18184296 | 105.5% |
Reaction Steps
A solution of 2-(5-fluorobenzofuran-3-yl)ethanol (5.2 g) and tetrabromomethane (11.6 g) in acetonitrile (175 mL) was treated with triphenylphosphine (8.3 g) at 0° C. After stirring for 15 min, the mixture was concentrated in vacuo an the resulting oil was applied to a silica gel flash column (eluent: heptane/ethyl acetate 65:35) resulting in an oil, 3-(2-bromoethyl)-5-fluorobenzofuran (7.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06596722B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-7583c66373cf4db1b81f2cf267946e17 |
| Source note | uspto-grants-2003_07 |