HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2,6-Difluorophenacyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-(2,6-Difluorophenyl)ethan-1-one | HCID 83643 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,6-Difluorophenacyl bromide | HCID 2778263 | 100% |
Reaction Steps
To a solution of 1-(2,6-difluorophenyl)ethanone (10.0 g) in diethyl ether (50 mL) was added anhydrous aluminum chloride (86 mg) and the mixture was stirred for 5 min. Bromine (3.3 mL) was added dropwise at 10-15° C. After stirring at room temperature for 2 hr, the mixture was poured into water, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, concentrated under reduced pressure to give the title compound as a pale-yellow oil (yield 15.2 g, about 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338462B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-c014dc2e3d79436b86a35ca1fdfc0b65 |
| Source note | uspto-grants-2012_12 |