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HRID 2653作成日:2026年10月25日

Water → 4-n-Heptyl-4-phenyl-4-silacyclohexane carbaldehyde

https://huagongshe.com/reaction/2653

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-n-Heptyl-4-phenyl-4-silacyclohexanoneHCID 19593797—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物4-n-Heptyl-4-phenyl-4-silacyclohexane carbaldehydeHCID 53830843—

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 28 g of 4-n-heptyl-4-phenyl-4-silacyclohexanone in 50 ml of THF was added to the solution. After agitation for 2 hours at room temperature, the mixture was poured into iced water and extracted with methylene chloride. The extract was washed, dried and concentrated by a usual manner. n-Hexane was added to the resultant concentrate, followed by removal of the resultant triphenylphosphine oxide crystals by filtration. The resultant filtrate was concentrated. The concentrate was hydrolyzed with 100 ml of 20% hydrochloric acid, followed by washing, drying and concentration by a usual manner to obtain 4-n-heptyl-4-phenyl-4-silacyclohexane 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-185154b6627f4f909d32b9149fae48a3
出典メモuspto-grants-1998_03