HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromophenol → 1-bromo-4-(1-ethoxyethoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Ethyl vinyl ether | HCID 8023 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-bromo-4-(1-ethoxyethoxy)benzene | HCID 2723761 | 100% |
Reaction Steps
p-Bromophenol (50 g, 0.29 mole), ethyl vinyl ether (41.7 g, 0.58 mole) and pyridinium p-toluenesulfonate (1.5 g) were dissolved in methylene chloride (300 ml), followed by reaction with stirring at room temperature for 6 hours. Then 5% aqueous sodium bicarbonate (400 ml) was added to the reaction mixture, and stirred. Then, the organic layer was separated, washed with H2O (300 ml×3), dried over anhydrous MgSO4 and evaporated. The residue (82 g) was distilled under reduced pressure to give 71.1 g of p-bromo-(1-ethoxyethoxy)benzene as a pale yellow oil having a boiling point of 112°-114° C./6 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05468589 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-a8c05469dbbe4c58a020ca1a81482b36 |
| Source note | uspto-grants-1995_11 |