Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triphenylsilanol → (2,6,6-Trimethyl-4-oxocyclohex-2-en-1-ylidene)acetaldehyde
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triphenylsilanol | HCID 69925 | — |
| 반응물 | 2-Cyclohexen-1-one, 4-ethynyl-4-hydroxy-3,5,5-trimethyl- | HCID 578890 | — |
| 촉매 | Stearic Acid | HCID 5281 | — |
| 촉매 | Vanadium | HCID 23990 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | (2,6,6-Trimethyl-4-oxocyclohex-2-en-1-ylidene)acetaldehyde | HCID 53790600 | 365.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05015779 |
| 출처 데이터셋 | uspto-grants-1991_05 |
| ORD ID | ord-0359fddf0abb462580cf59fabb0bbe63 |
| 출처 메모 | uspto-grants-1991_05 |