HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128483Generated: October 26, 2026
Ethyl Lactate → Ethyl 2-(5-fluoro-2-nitrophenoxy)propanoate
https://huagongshe.com/reaction/128483
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Lactate | HCID 7344 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4-Difluoronitrobenzene | HCID 67967 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 2-(5-fluoro-2-nitrophenoxy)propanoate | HCID 19786322 | — |
Reaction Steps
2,4-Difluoronitrobenzene (16.9 g; 0.10 mole), ethyl lactate (11.8 g; 0.10 mole), and anhydrous potassium carbonate (13.8 g, 0.10 mole) are combined in dioxane (200 ml) and the temperature is brought to 95° C. over a 1.5 hour period and maintained at 95° C. for 3 hours. The reaction mixture is cooled to room temperature, the inorganic solids removed by filtration and the solvent removed under vacuum to afford a dark colored oil, from which low boiling fractions are removed by distillation (bp., 79° C./0.5 mm). The pot residue is then cooled to afford 15.9 g of crude product, which is recrystallized from ligroin/acetone to afford ethyl 2-(5-fluoro-2-nitrophenoxy)propionate as yellow needles, m.p. 64°-65° C. Elemental anal. Calcd for C11H12FNO5 : C, 51.4; H, 4.70; F, 7.38; N, 5.45. Found: C, 51.35; H, 4.74; F, 7.60; N, 5.44.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04259510 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-67f4c244bd2a4220b9f4d616e304c920 |
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| Source note | uspto-grants-1981_03 |
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