Zurück
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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(4-Pyridinyl)-2-cyclohexen-1-one oximeHCID 3017458—
EduktEthyl 2-(isonicotinoyl)-5-oxohexanoateHCID 9835014—
ProduktHCID 20295955HCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04246420
Quelldatensatzuspto-grants-1981_01
ORD IDord-4186e24c16a04a0e89cc140240a5414c
Quellennotizuspto-grants-1981_01