돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1684444생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1684444

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Sodium HydroxideHCID 14798—
반응물Methane, dichloromethoxy-HCID 21004—
반응물9-Borabicyclo(3.3.1)nonaneHCID 78966—
반응물Bicyclo(3.3.1)nonan-9-oneHCID 86638—
반응물n-PentylphenyldivinylsilaneHCID 19039141—
반응물2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매WaterHCID 962—
용매HexaneHCID 8058—
용매Tetrahydrofuran hexaneHCID 21883165—
생성물4-Pentyl-4-phenyl-4-silacyclohexanoneHCID 1107620591%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05641431
출처 데이터셋uspto-grants-1997_06
ORD IDord-f175e89148cd417692d0144a07b154ff
출처 메모uspto-grants-1997_06