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Triphenylsilanol → (2,6,6-Trimethyl-4-oxocyclohex-2-en-1-ylidene)acetaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triphenylsilanol | HCID 69925 | — |
| 反応物 | 2-Cyclohexen-1-one, 4-ethynyl-4-hydroxy-3,5,5-trimethyl- | HCID 578890 | — |
| 触媒 | Stearic Acid | HCID 5281 | — |
| 触媒 | Vanadium | HCID 23990 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | (2,6,6-Trimethyl-4-oxocyclohex-2-en-1-ylidene)acetaldehyde | HCID 53790600 | 365.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05015779 |
| 出典データセット | uspto-grants-1991_05 |
| ORD ID | ord-0359fddf0abb462580cf59fabb0bbe63 |
| 出典メモ | uspto-grants-1991_05 |