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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289348Generated: October 30, 2026

Ethyl Acetate → Methyl 4-(glycidyloxy)-2-(2,2,2-trifluoroethoxy)-phenylacetate

https://huagongshe.com/reaction/2289348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
ReactantEpibromohydrinHCID 18430—
ReactantHCID 18700130HCID 18700130—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-(glycidyloxy)-2-(2,2,2-trifluoroethoxy)-phenylacetateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090805
Source datasetuspto-grants-2000_07
ORD IDord-15f30d2556624e8090804fd49406fc62
Source noteuspto-grants-2000_07