HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1389915Erstellt: 25. Oktober 2026
3-(4-Pyridinyl)-2-cyclohexen-1-one oxime → HCID 20295955, Verbindung
https://huagongshe.com/reaction/1389915
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-(4-Pyridinyl)-2-cyclohexen-1-one oxime | HCID 3017458 | — |
| Edukt | Ethyl 2-(isonicotinoyl)-5-oxohexanoate | HCID 9835014 | — |
| Produkt | HCID 20295955 | HCID 20295955 | — |
Reaktionsschritte
An improvement in the process for preparing 3-(4-pyridinyl)-2-cyclohexen-1-one oxime by heating ethyl 5-oxo-2-[(4-pyridinyl)carbonyl]hexanoate under aqueous acidic conditions to produce 1-(4-pyridinyl)-hexan-1,5-dione, heating said hexan-1,5-dione with a basic condensing agent to produce 3-(4-pyridinyl)-2-cyclohexen-1-one, and converting said cyclohexen-1-one to its oxime, said improvement being a one pot sequence consisting of first heating ethyl 5-oxo-2-[(4-pyridinyl)carbonyl]hexanoate with excess aqueous sulfuric acid, neutralizing the excess acid, shaking the resulting warm mixture well with isopropyl alcohol to extract the 3-(4-pyridinyl)-2-cyclohexen-1-one, draining off the heavier warm aqueous layer, adding hydroxylamine hydrochloride to the isopropyl alcohol solution of 3-(4-pyridinyl)-2-cyclohexen-1-one, stirring the mixture at reflux, basifying the mixture and evaporating the reaction mixture to dryness, and isolating the 3-(4-pyridinyl)-2-cyclohexen-1-one oxime from the residue.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04246420 |
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| Quelldatensatz | uspto-grants-1981_01 |
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| ORD ID | ord-4186e24c16a04a0e89cc140240a5414c |
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| Quellennotiz | uspto-grants-1981_01 |
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