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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42729Erstellt: 24. Oktober 2026

Pyridine → 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone O-methyl-oxime

https://huagongshe.com/de/reaction/42729

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktO-Methylhydroxylamine hydrochlorideHCID 521874—
Edukt1-(2,2,4-Trimethyl-3-cyclohexen-1-yl)ethan-1-oneHCID 3016988—
LösungsmittelMethanolHCID 887—
Produkt1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone O-methyl-oximeHCID 8667533892,4%

Reaktionsbedingungen

Temperatur24 °C

Reaktionsschritte

To a stirred solution of 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone (162 g; 0.97 mol), prepared as described in example P4, in methanol (500 ml) was added pyridine (160 ml; 1.95 mol) followed by a portionwise addition of methoxyamine hydrochloride (142 g; 1.70 mol). The reaction mixture was stirred at 24° C. for 16 hours under nitrogen atmosphere. Methanol was removed under reduced pressure, the residue poured in water (600 ml) and 1N hydrochloric acid was added (100 ml). The solution was extracted with dichloromethane (3×300 ml). Combined organic layers were washed with brine (500 ml) and dried over sodium sulfate. The solvent was removed in vacuo to afford 175 g (92% of theory) of 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone O-methyl-oxime as a clear red oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536215B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-949bef1b62f54a69bbcb37a365ea0c46
Quellennotizuspto-grants-2013_09