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HRID 1588146作成日:2026年10月26日

Metasilicic acid → Tridec-5-ene

https://huagongshe.com/reaction/1588146

反応式

関与物質

役割名称HCID仕込み量
反応物Metasilicic acidHCID 14768—
反応物Acetonitrile--water (1/1)HCID 18373917—
反応物1-[2,5-Dimethoxy-3,6-bis(methoxymethoxy)phenyl]tridec-8-yneHCID 19757187—
触媒Palladium-barium sulfate quinolineHCID 131717989—
溶媒MethanolHCID 887—
生成物Tridec-5-eneHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05220042
出典データセットuspto-grants-1993_06
ORD IDord-88220a06a0304de1b1f78196c495755d
出典メモuspto-grants-1993_06