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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Ethyl Glycolate | HCID 12184 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 1,2-Dichloro-4-fluoro-5-nitrobenzene | HCID 533951 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | Ethyl[(4,5-dichloro-2-nitrophenyl)oxy]acetate | HCID 44203104 | 96.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07749998B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-2fa426fcf11247078ba85815428ea13a |
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| Source note | uspto-grants-2010_07 |
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