HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Benzyloxy-5-(trifluoromethoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | p-(Trifluoromethoxy)phenol | HCID 70015 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Benzyloxy-5-(trifluoromethoxy)benzene | HCID 21584094 | 99% |
Reaction Steps
Benzyl bromide (66.17 ml, 95.35 g, 0.56 mol) was added to a mixture of 4-(trifluoromethoxy)phenol (90.26 g, 0.51 mol) and potassium carbonate (140.97 g, 1.2 mol) in dimethylformamide (160 ml) and the mixture was stirred at room temperature for 72 hours. The mixture was poured into water (1.5 l) and extracted with ethyl acetate (3×50 ml). The combined organic fractions were washed with aqueous sodium carbonate (saturated, 500 ml), dried (MgSO4) and the solvent was evaporated under reduced pressure to give the title compound as a colorless solid (133.5 g, 99%). 1H NMR (360 MHz, CDCl3) δ 7.39 (5H, m), 7.14 (2H, d, J=9.0 Hz), 6.95 (2H, d, J=9.0 Hz), and 5.05 (2H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05919781 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-e7ce170568e942388efb1fa9100cad31 |
| Source note | uspto-grants-1999_07 |