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HRID 1382699作成日:2026年10月25日

Pentyltriphenylphosphonium bromide → 1-(4-Nonylphenyl)-hex-1-ene

https://huagongshe.com/reaction/1382699

反応式

関与物質

役割名称HCID仕込み量
反応物Pentyltriphenylphosphonium bromideHCID 2724565—
反応物4-NonylbenzaldehydeHCID 10933364—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物1-(4-Nonylphenyl)-hex-1-eneHCID 53676959—

反応手順

A suspension of 13.9 g of pentyltriphenylphosphonium bromide in 150 ml of tetrahydrofuran is cooled to -20° under argon, 21.2 ml of 1.6M butyllithium solution in hexane are added within a period of 5 minutes and the whole is stirred for a further 30 minutes at 0°-10°. 6 g of 4-nonylbenzaldehyde in 40 ml of tetrahydrofuran are added dropwise over a period of 30 minutes to the mixture, which has been cooled to from -60° to -70°. The reaction mixture is allowed to warm spontaneously to 0°-10°, stirred at this temperature for a further 45 minutes and concentrated by evaporation. The residue is taken up in hexane/ethyl acetate (1:) and filtered over silica gel. The filtrate is concentrated by evaporation and chromatographed on silica gel with hexane. The title compound (mixture of cis- and trans-isomers) is obtained in the form of a colourless oil, which is used directly in the next stage.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04808572
出典データセットuspto-grants-1989_02
ORD IDord-1684badff4fe41d6879673bc35815f6b
出典メモuspto-grants-1989_02