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HRID 1197374作成日:2026年10月25日

Tetrabutylammonium Fluoride → 1-(Hex-5-ynyl)-4-n-propyl-2,6-dioxabicyclo[2.2.2]octane

https://huagongshe.com/reaction/1197374

反応式

関与物質

役割名称HCID仕込み量
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物4-n-Propyl-1-(6-trimethylsilylhex-5-ynyl) 2,6-dioxabicyclo[2.2.2]octaneHCID 19373370—
溶媒TetrahydrofuranHCID 8028—
生成物1-(Hex-5-ynyl)-4-n-propyl-2,6-dioxabicyclo[2.2.2]octaneHCID 19373289—

反応手順

Tetrabutylammonium fluoride solution (1.0M., solution 4.0 ml.) was added to a stirred solution of 4-n-propyl-1-(6-trimethylsilylhex-5-ynyl)-2,6,-dioxabicyclo[2.2.2]octane in dry tetrahydrofuran (40 ml.) at 20° and the mixture was stirred for 1 hour. The solvent was removed in vacuo and the residue was extracted with diethyl ether and water. The ethereal extracts were dried over anhydrous magnesium sulphate and evaporated in vacuo. The residue was chromatographed on alumina eluting with dichloromethane:hexane 1:9, saturated with ammonia. 1-(Hex-5-ynyl)-4-n-propyl-2,6-dioxabicyclo[2.2.2]octane was obtained as a colourless oil (0.45 g.)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05116862
出典データセットuspto-grants-1992_05
ORD IDord-85ee9095fa5e42559ffa6cb49e552239
出典メモuspto-grants-1992_05