HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-(4-Bromo-2,6-dimethylphenoxy)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl (4-bromo-2,6-dimethylphenoxy)acetate | HCID 875019 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Bromo-2,6-dimethylphenoxy)ethanol | HCID 53707443 | 96.6% |
Reaction Steps
Sodium borohydride (0.206 g) was added to a mixture of ethyl(4-bromo-2,6-dimethylphenoxy)acetate (0.782 g), tetrahydrofuran (5 mL) and ethanol (5 mL), and the mixture was stirred at room temperature for 4 hrs. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/2) to afford the title compound (0.645 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07417169B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-39dba05a1b9b441197d4fa26af2ce661 |
| Source note | uspto-grants-2008_08 |