関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Metasilicic acid | HCID 14768 | — |
| 反応物 | Acetonitrile--water (1/1) | HCID 18373917 | — |
| 反応物 | 1-[2,5-Dimethoxy-3,6-bis(methoxymethoxy)phenyl]tridec-8-yne | HCID 19757187 | — |
| 触媒 | Palladium-barium sulfate quinoline | HCID 131717989 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Tridec-5-ene | HCID 141217 | — |
反応手順
1 Gram of 1-[2,5-dimethoxy-3,6-bis(methoxymethoxy)phenyl]tridec-8-yne prepared in the above-mentioned (2) was dissolved in 10 ml of methanol, to this solution was added 40 mg of 5%-palladium-barium sulfate-quinoline (1:1) and the mixture was catalytically reduced under a normal hydrogen pressure at room temperature for 4 hours. This reaction was traced by means of a high performance liquid chromatography. Thus, the reaction was determined by measuring the optical density (OD) at UV254 under conditions of ODS column, 80%-acetonitrile-water, 2 ml/minute. After the reaction was completed, the catalyst was removed by filtration, and methanol was removed by evaporation under reduced pressure, and the residue obtained was treated by means of a column chromatography ("Robar " column, LiChrosorb RP-8, Type C, manufactured by E. Merck A. G.) and eluted with 75%-acetonitrile-water at the flow rate of 5 ml/minute to obtain both Z-isomer and E-isomer, respectively. There was obtained 0.65 g of 1-[2,5-dimethoxy-3,6-bis-Imethoxymethoxy)phenyl]tridec-8 -ene (Z-isomer) as in the form of colorless oily substance.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05220042 |
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| 出典データセット | uspto-grants-1993_06 |
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| ORD ID | ord-88220a06a0304de1b1f78196c495755d |
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| 出典メモ | uspto-grants-1993_06 |
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