HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2261728Erstellt: 26. Oktober 2026
Hydrochloric Acid → 3-Acetyl-2-methoxyimino-5-methyl-hexanoic acid ethyl ester
https://huagongshe.com/reaction/2261728
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Isobutyl iodide | HCID 10556 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Ethyl 2-(methoxyimino)-4-oxopentanoate | HCID 589173 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 3-Acetyl-2-methoxyimino-5-methyl-hexanoic acid ethyl ester | HCID 76540076 | 29,4% |
Reaktionsschritte
To a solution of 2-methoxyimino-4-oxo-pentanoic acid ethyl ester (2.62 g, 14 mmol) in DMF (30 mL) is added potassium carbonate (2.5 g, 18.2 mmol) followed by 1-iodo-2-methyl-propane (1.62 mL, 14 mmol) and the mixture is stirred at ambient temperature overnight. Additional 1-iodo-2-methyl-propane (0.8 mL, 7 mmol) is added and the mixture is stirred at 60° C. for 1 hour. The reaction mixture is diluted with EtOAc and is adjusted to pH 3 with 1N HCl. The organic layer is washed with brine, dried (MgSO4), filtered, and concentrated under reduced pressure. The residue is purified by column chromatography (0 to 20% EtOAc in hexanes) to give the title compound as a colorless oil (1 g, 29%). 1H NMR (400 MHz, CDCl3) δ 4.33 (q, 2H), 4.06 (s, 3H), 4.03 (dd, 1H), 2.07 (s, 3H), 1.88 (m, 1H), 1.58 (m, 1H), 1.43 (m, 1H), 1.37 (t, 3H), 0.89 (d, 6H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07846960B2 |
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| Quelldatensatz | uspto-grants-2010_12 |
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| ORD ID | ord-83f7b6a6cfc84cdeb6d1a0b0560ad9f0 |
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| Quellennotiz | uspto-grants-2010_12 |
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