HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 2-(Trifluoromethoxy)benzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-(Trifluoromethoxy)benzyl alcohol | HCID 2777245 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(Trifluoromethoxy)benzyl bromide | HCID 2777254 | — |
Reaction Steps
To a stirred solution of 2-trifluoromethoxybenzyl alcohol (0.81 g, 4.5 mmol) from Step 1 above in ether (20 mL) at 0° C. was added triphenylphosphine (2.4 g, 9.2 mmol) and CBr4 (3.0 g, 9.2 mmol). The mixture was warmed to ambient temperature and stirred for 18 h. The ether was decanted from the gummy precipitate of triphenylphosphine oxide and evaporated under reduced pressure. The residue was purified by pressurized silica gel column chromatography using hexanes as eluant to give 2-trifluoromethoxybenzyl bromide as a colorless liquid (TLC Rf =0.80 (hexanes)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05968938 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-9121b104c65a455fa81be3fc4bb025dd |
| Source note | uspto-grants-1999_10 |