HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2-Bromo-3,5-difluorophenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 3,5-Difluorophenol | HCID 75928 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | 2-Bromo-3,5-difluorophenol | HCID 22144860 | 60% |
Reaction Steps
A solution of 2.6 gm (20 mmol) 3,5-difluorophenol in 20 mL carbon disulfide was cooled to 0° C. and then a solution of 1.02 mL (20 mMol) bromine in 10 mL carbon disulfide was added dropwise over 30 minutes. After stirring for an additional 30 minutes, the reaction mixture was warmed to room temperature and stirred for 1.5 hours. The reaction mixture was diluted with 200 mL diethyl ether and was washed sequentially with aqueous sodium metabisulfite and saturated aqueous sodium chloride. The organic phase was then dried over sodium sulfate and concentrated under reduced pressure. The residue was vacuum distilled to provide 2.5 gm (60%) of 2-bromo-3,5-difluorophenol (b.p.=65° C. (5 mm Hg)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07045545B1 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-e9581c03b5c94f1fa40f5f6e2858cee5 |
| Source note | uspto-grants-2006_05 |