HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490746Generated: October 29, 2026
Ammonium Acetate → HCID 69053468, compound
https://huagongshe.com/reaction/490746
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 69056835 | HCID 69056835 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 69053468 | HCID 69053468 | 50% |
Reaction Steps
4-Trifluoromethyl-benzoic acid 3-ethoxycarbonyl-1-ethyl-2-oxo-propyl ester (25 mmol) is dissolved in acetic acid (100 mL) and dry ammonium acetate (10 g, 100 mmol) is added, then the reaction is heated under nitrogen to reflux. The reaction is monitored by TLC and HPLC but complete consumption of the starting material is never observed, and then allowed to cool. The cooled reaction is concentrated and diluted with 250 mL ethyl acetate. The residue is washed with 100 mL saturated sodium bicarbonate followed by water and brine. The organic layer is dried over anhydrous sodium sulfate, then concentrated and purified by column chromatrography. The fractions that contained pure product are concentrated to yield [5-Ethyl-2-(4-trifluoromethyl-phenyl)-oxazol-4-yl]-acetic acid ethyl ester (4.0 g, 12.22 mmol) or 50% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528160B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-f7764afe4a174d378113c6b952c7690a |
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| Source note | uspto-grants-2009_05 |
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