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HRID 2658作成日:2026年10月25日

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

https://huagongshe.com/reaction/2658

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
反応物4-(4-n-Pentyl-4-phenyl-4-silacyclohexyl)cyclohexanoneHCID 11067854—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物4-(4-Phenyl-4-n-pentyl-4-silacyclohexyl)cyclohexane carbaldehydeHCID 53863304—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05730901
出典データセットuspto-grants-1998_03
ORD IDord-60ff9b3f88b74fb89fc2c3b2f2e968f6
出典メモuspto-grants-1998_03