HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,2-Bis-benzyloxy-3-bromo-5-trifluoromethyl-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,2-Benzenediol, 3-bromo-5-(trifluoromethyl)- | HCID 59643037 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,2-Bis-benzyloxy-3-bromo-5-trifluoromethyl-benzene | HCID 59643024 | — |
Reaction Steps
To a solution of 3-bromo-5-trifluoromethyl-benzene-1,2-diol (510 mg, 1.98 mmol) in 10 mL acetone, K2CO3 (2.74 g, 19.84 mmol, 10 eq.) and benzyl bromide (1.02 g, 5.95 mmol, 3 eq.) were added and the solution was refluxed for 4 h. After cooling to r.t., H2O and EtOAc were added to the mixture and the phases were separated The organic fraction was washed with saturated NaCl solution, dried over MgSO4 and evaporated in vacuo. The crude product was purified using flash chromatography (silica gel, hexane/EtOAc 10:1) to yield the title compound as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07319101B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-358d3336000e4671bd5237234139eec0 |
| Source note | uspto-grants-2008_01 |