関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pentyltriphenylphosphonium bromide | HCID 2724565 | — |
| 反応物 | 4-Nonylbenzaldehyde | HCID 10933364 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 1-(4-Nonylphenyl)-hex-1-ene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04808572 |
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| 出典データセット | uspto-grants-1989_02 |
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| ORD ID | ord-1684badff4fe41d6879673bc35815f6b |
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| 出典メモ | uspto-grants-1989_02 |
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