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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2051056Erstellt: 23. Oktober 2026

Triphenylsilanol → (2,6,6-Trimethyl-4-oxocyclohex-2-en-1-ylidene)acetaldehyde

https://huagongshe.com/de/reaction/2051056

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylsilanolHCID 69925—
EduktHCID 578890HCID 578890—
KatalysatorStearic AcidHCID 5281—
KatalysatorVanadiumHCID 23990—
LösungsmittelO-XyleneHCID 7237—
Produkt(2,6,6-Trimethyl-4-oxocyclohex-2-en-1-ylidene)acetaldehydeHCID 53790600365,2%

Reaktionsschritte

Triphenylsilanol (22 g) and 80 g (0.45 mol) of 3,5,5-trimethyl-4-hydroxy-4-ethynylcyclohex-2-en-1-one and 1.6 g of stearic acid are dissolved in 800 ml of xylene, treated with 1.92 ml of vanadium isopropylate and heated to reflux temperature while stirring. After 31/2 hours the reaction mixture is cooled and washed with 5% sodium bicarbonate, whereby an emulsion results. The organic phase is then separated, the emulsion is also separated and extracted with ether. The organic phases are dried over magnesium sulphate and concentrated. The residue (117.9 g) is distilled (oil bath 130°-170°; 0.001 mm Hg). In this manner there are obtained 51.8 g (64.8%) of (2,6,6-trimethyl-4-oxo-2-cyclohexen-1-ylidene)acetaldehyde (Z:E=about 3:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05015779
Quelldatensatzuspto-grants-1991_05
ORD IDord-0359fddf0abb462580cf59fabb0bbe63
Quellennotizuspto-grants-1991_05