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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354316Generated: October 25, 2026

Trifluoroacetic acid → Ethyl[(4,5-dichloro-2-nitrophenyl)oxy]acetate

https://huagongshe.com/reaction/2354316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl GlycolateHCID 12184—
ReactantPotassium FluorideHCID 522689—
Reactant1,2-Dichloro-4-fluoro-5-nitrobenzeneHCID 533951—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductEthyl[(4,5-dichloro-2-nitrophenyl)oxy]acetateHCID 4420310496.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

1,2-dichloro-4-fluoro-5-nitrobenzene (50 g, 0.238 mol), ethyl glycolate (90.1 mL, 0.952 mol), and potassium fluoride (76.1 g, 1.31 mol) were added to a 1 L round-bottom flask containing 200 mL of anhydrous dioxane. The mixture was magnetically stirred and heated to 100° C. in an oil bath. After two hours, HPLC (Eclipse XDB-C18, 4.6×250 mm, 5 micron, 1-99% CH3CN/H2O with 0.1% trifluoroacetic acid) showed that all of the starting material (Rt=7.5 min) was gone and that one major peak (Rt=7.8 min) had formed. The reaction mixture was poured into 4 L of water, which resulted in precipitation of the product. The solid was filtered off and dried under vacuum to give ethyl[(4,5-dichloro-2-nitrophenyl)oxy]acetate (67.4 g, 0.229 mol, 96%) as a tan solid. MS (ES) m/e 294 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749998B2
Source datasetuspto-grants-2010_07
ORD IDord-2fa426fcf11247078ba85815428ea13a
Source noteuspto-grants-2010_07