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HRID 1684444作成日:2026年10月27日

Hydrogen Peroxide → 4-Pentyl-4-phenyl-4-silacyclohexanone

https://huagongshe.com/reaction/1684444

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物Sodium HydroxideHCID 14798—
反応物Methane, dichloromethoxy-HCID 21004—
反応物9-Borabicyclo(3.3.1)nonaneHCID 78966—
反応物Bicyclo(3.3.1)nonan-9-oneHCID 86638—
反応物n-PentylphenyldivinylsilaneHCID 19039141—
反応物2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒HexaneHCID 8058—
溶媒Tetrahydrofuran hexaneHCID 21883165—
生成物4-Pentyl-4-phenyl-4-silacyclohexanoneHCID 1107620591%

反応条件

温度0 °C

反応手順

A mixture of 15.9 g of 9-borabicyclo [3.3.1] nonan, 14.8 g of n-pentylphenyldivinylsilane and 150 ml of n-hexane was refluxed for 2 hours and then cooled with ice water. 7.0 ml of borane-dimethylsufide was added to the mixture, which was then heated again and refluxed for 2 hours. After cooling, 16 ml of methanol was added at room temperature and the mixture was stirred for 2 hours at 0° C. 25.0 g of dichloromethylmethyl ether was then dripped into the mixture, followed by also dripping a hexane-tetrahydrofuran (1:1) solution of 1.33M lithium t-butoxide into the mixture. After stirring at room temperature for 2 hours, 80 ml of ethanol, 10 ml of water and 10.0 g of sodium hydroxide were added. Then 80 ml of an aqueous solution of 30% hydrogen peroxide was slowly added. After stirring at room temperature for 2 hours, the organic layer was dried/concentrated to obtain a mixture of the target product and bicyclo [3.3.1] nonan-9-one. They were separated by means of silica-gel chromatography to obtain 15.2 g (yield 91%) of the target product. The target product thus obtained exhibited the same spectra as those of Example 7.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05641431
出典データセットuspto-grants-1997_06
ORD IDord-f175e89148cd417692d0144a07b154ff
出典メモuspto-grants-1997_06