HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23521Generated: October 29, 2026
Pivalaldehyde → HCID 12997788, compound
https://huagongshe.com/reaction/23521
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pivalaldehyde | HCID 12417 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 1-(2-Fluoropyridin-4-yl)-2-(4-fluorophenyl)ethane-1,2-dione-1-oxime | HCID 136335780 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 12997788 | HCID 12997788 | — |
Reaction Steps
To a solution of 1-(4-fluorophenyl)-2-(2-fluoropyridin-4-yl)ethane-1,2-dione 2-oxime (47.3 g, 0.18 mol) in acetic acid (1 L) under nitrogen was added trimethylacetaldehyde (21.6 mL, 0.19 mol) followed by ammonium acetate (277.5 g, 3.6 mol) and then it was heated to reflux for three hours. The acetic acid was removed under reduced pressure and the remaining material was taken up in water. The pH of the solution was adjusted to 8-10 by addition of solid ammonium hydroxide and was extracted with EtOAc. The solvent was removed under reduced pressure and the crude product was dissolved in methanol with sufficient ethanol added to effect dissolution. The solvent was removed under reduced pressure; the product was twice dissolved in ethanol and concentrated to a small volume under reduced pressure to azeotropically remove water. The title compound was recrystallized from ethanol and hexane (28.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852727B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-98fbbf205b954765abec2a43e450a43f |
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| Source note | uspto-grants-2005_02 |
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