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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1460830생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/1460830

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylsilanolHCID 69925—
반응물2-Cyclohexen-1-one, 4-ethynyl-4-hydroxy-3,5,5-trimethyl-HCID 578890—
촉매Stearic AcidHCID 5281—
촉매VanadiumHCID 23990—
용매O-XyleneHCID 7237—
생성물(2,6,6-Trimethyl-4-oxocyclohex-2-en-1-ylidene)acetaldehydeHCID 53790600365.2%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05072019
출처 데이터셋uspto-grants-1991_12
ORD IDord-df58c5fc2fb048dfb99c08bf4e1c387a
출처 메모uspto-grants-1991_12