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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2658생성일: 2026년 10월 27일

Water → 4-(4-Phenyl-4-n-pentyl-4-silacyclohexyl)cyclohexane carbaldehyde

https://huagongshe.com/reaction/2658

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
반응물4-(4-n-Pentyl-4-phenyl-4-silacyclohexyl)cyclohexanoneHCID 11067854—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물4-(4-Phenyl-4-n-pentyl-4-silacyclohexyl)cyclohexane carbaldehydeHCID 53863304—

반응 단계

12 g of potassium t-butoxide was added to a mixture of 35 g of methoxymethyltriphenylphosphonium chloride and 200 ml of THF to prepare an orange ylide solution. A solution of 34 g of 4-(4-n-pentyl-4-phenyl-4-silacyclohexyl)cyclohexanone in 50 ml of THF was added to the ylide solution and agitated at room temperature for 2 hours. Thereafter, the mixture was poured into iced water and extracted with methylene chloride, followed by washing, drying and concentration by a usual manner. n-Hexane was added to the residue, and the resultant crystals of triphenylphosphine oxide were removed by filtration. The filtrate was concentrated, and the resultant residue was hydrolyzed with 100 ml of 20% hydrochloric acid, followed by washing, drying and concentration by a usual manner to obtain 4-(4-n-pentyl-4-phenyl-4-silacyclohexyl)cyclohexane carbaldehyde.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05730901
출처 데이터셋uspto-grants-1998_03
ORD IDord-60ff9b3f88b74fb89fc2c3b2f2e968f6
출처 메모uspto-grants-1998_03