HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethanol → 2-(3-BroMo-phenoxy)-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromophenol | HCID 11563 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(3-BroMo-phenoxy)-ethanol | HCID 10536727 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
In a nitrogen atmosphere, 3-bromophenol 5.0 g, 2-bromoethanol 5.42 g, and potassium carbonate 12.0 g were added to N,N-dimethylformamide 30 ml, and the mixture was stirred at 100° C. After 1 hour, the reaction mixture was cooled to room temperature and partitioned by adding water and diethyl ether. The organic layer was washed with water and then with brine, dried over magnesium sulfate anhydride and evaporated. The residue was purified by silica gel column chromatography (hexane/ethyl acetate system), whereby the title compound (4.85 g, 77%) was obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06737425B1 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-150c977ffbf2411da004a9b09b492068 |
| Source note | uspto-grants-2004_05 |