HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → Methyl 4-(glycidyloxy)-2-(2,2,2-trifluoroethoxy)-phenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Epibromohydrin | HCID 18430 | — |
| Reactant | HCID 18700130 | HCID 18700130 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-(glycidyloxy)-2-(2,2,2-trifluoroethoxy)-phenylacetate | HCID 53968277 | — |
Reaction Steps
To a stirred solution of methyl 4-hydroxy-2-(2,2,2-trifluoroethoxy)phenylacetate (0.60 g, 2.4 mmol) from Step 4 of Example 32 in DMF (7 mL) was added epibromohydrin (0.50 g, 3.6 mmol) and Cs2CO3 (1.55 g, 4.8 mmol). The mixture was stirred at ambient temperature for 3 h. EtOAc was added (15 mL) and the solid was removed by filtration. The filtrate solvents were removed under reduced pressure and the residue was partitioned between EtOAc (50 mL) and saturated aqueous NaHCO3 (50 mL). The organic phase was dried (MgSO4), filtered, and the solvent was removed under reduced pressure to give methyl 4-(glycidyloxy)-2-(2,2,2-trifluoroethoxy)-phenylacetate as a pale yellow oil (HPLC retention time=8.3 min (method A)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06090805 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-15f30d2556624e8090804fd49406fc62 |
| Source note | uspto-grants-2000_07 |