HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2,6-Difluorophenacyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-(2,6-Difluorophenyl)ethan-1-one | HCID 83643 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2,6-Difluorophenacyl bromide | HCID 2778263 | — |
Reaction Steps
40.6 g of 2,6-difluoroacetophenone are placed in 120 ml of chloroform, and 0.1 g of aluminium chloride is added. Then, at 0° C., 37 g of bromine in 240 ml of chloroform are added dropwise and stirring is carried out at 0° C. for 1 h. The reaction mixture is then heated to room temperature and is concentrated using a rotary evaporator. The residue is distilled over a Vigreux column. In this way 2-bromo-1-(2,6-difluorophenyl)-ethanone having a boiling point of 101-11° C. at 9 mbar is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06723720B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-ab6e108662d2435aa647c363a9716f4e |
| Source note | uspto-grants-2004_04 |