HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Fluorotoluene → 4-Fluorobenzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Fluorotoluene | HCID 9603 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-Fluorobenzyl bromide | HCID 68021 | 101.1% |
Reaction Steps
A 300-ml flask was charged with 16.6 g of 4-fluorotoluene, 30.0 g of NBS, 0.5 g of benzoyl peroxide and 150 ml of carbon tetrachloride, and the mixture was refluxed for 2.0 hours. The reaction mixture was cooled to room temperature, and the formed precipitate was removed by filtration and the residual CCl4 solution was washed with dilute alkali and then with water, dried over Na2SO4, and evaporated under reduced pressure to give 28.8 g of crude 4-fluorobenzyl bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04397864 |
| Source dataset | uspto-grants-1983_08 |
| ORD ID | ord-488f31c16d854192accd904c27116779 |
| Source note | uspto-grants-1983_08 |