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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460830Generated: October 26, 2026

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

https://huagongshe.com/reaction/1460830

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 numberUS05072019
Source datasetuspto-grants-1991_12
ORD IDord-df58c5fc2fb048dfb99c08bf4e1c387a
Source noteuspto-grants-1991_12