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HRID 2051056作成日:2026年10月27日

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

https://huagongshe.com/reaction/2051056

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylsilanolHCID 69925—
反応物2-Cyclohexen-1-one, 4-ethynyl-4-hydroxy-3,5,5-trimethyl-HCID 578890—
触媒Stearic AcidHCID 5281—
触媒VanadiumHCID 23990—
溶媒O-XyleneHCID 7237—
生成物(2,6,6-Trimethyl-4-oxocyclohex-2-en-1-ylidene)acetaldehydeHCID 53790600365.2%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05015779
出典データセットuspto-grants-1991_05
ORD IDord-0359fddf0abb462580cf59fabb0bbe63
出典メモuspto-grants-1991_05