HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromophenol → 1-Bromo-2-[2-(4-fluorophenyl)ethoxy]benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromophenol | HCID 7244 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 4-Fluorophenethyl Alcohol | HCID 82068 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Bromo-2-[2-(4-fluorophenyl)ethoxy]benzene | HCID 21914340 | 75.7% |
Reaction Steps
2-Bromophenol (3.46 g) was mixed with tetrahydrofuran (60 ml) and triphenylphosphine (6.3 g) was added along with 4-fluorophenethyl alcohol (4.2 g). The mixture was cooled in an ice bath before dropwise addition of diisopropyl azodicarboxylate (4.85 g). The mixture was allowed to warm to room temperature over 18 h. The mixture was evaporated and diethyl ether (100 ml) was added. Stirring was continued for 3 h, the mixture was filtered and the filtrate was evaporated. The product was purified by column chromatography eluting with ethyl acetate/hexane mixtures to give a yellow oil (4.47 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07125896B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-907b4dfff61f407080ed1e9bfa8c5e05 |
| Source note | uspto-grants-2006_10 |