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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051056Generated: October 23, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylsilanolHCID 69925—
Reactant2-Cyclohexen-1-one, 4-ethynyl-4-hydroxy-3,5,5-trimethyl-HCID 578890—
CatalystStearic AcidHCID 5281—
CatalystVanadiumHCID 23990—
SolventO-XyleneHCID 7237—
Product(2,6,6-Trimethyl-4-oxocyclohex-2-en-1-ylidene)acetaldehydeHCID 53790600365.2%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05015779
Source datasetuspto-grants-1991_05
ORD IDord-0359fddf0abb462580cf59fabb0bbe63
Source noteuspto-grants-1991_05