HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2'-Fluoro-4'-iodophenacyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2'-Fluoro-4'-iodoacetophenone | HCID 53415454 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2'-Fluoro-4'-iodophenacyl bromide | HCID 87232768 | 99.2% |
Reaction Steps
A solution of bromine (2.74 mL, 53.18 mmol) in acetic acid (30 mL) was added dropwise to a solution of 1-(2-fluoro-4-iodo-phenyl)-ethanone (14.04 g, 53.18 mmol) in acetic acid (200 mL) at room temperature under an atmosphere of nitrogen and then stirred for 24 hours. The reaction was concentrated to near dryness in vacuo, diluted with ethyl acetate (200 mL) and basified with saturated aqueous sodium carbonate solution. The organic layer was washed with brine, dried over sodium sulfate, filtered through a pad of silica gel and concentrated in vacuo to give 2-bromo-1-(2-fluoro-4-iodo-phenyl)-ethanone (18.10 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063085B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-4717d0ca9600477c806380aa438c14b3 |
| Source note | uspto-grants-2011_11 |